Qoovee'de toptan Veterinerlik ve hayvan yemi

ОСОБЕННОСТИ И ПРЕИМУЩЕСТВА: • Позволяет защитить животное не только от блох, вшей, власоедов и клещей, а также от нематод.• Широкий спектр действия на личиночные и половозрелые стадии экто- и эндопаразитов.• Широкий диапазон размеров – 40 – 80 см.• Фипронил обеспечивает длительное контактное инсектоакарицидное действие.• Ивермектин, накапливаясь в эпидермисе, действует на наружных паразитов; частично всасываясь в кровь, попадает в системный кровоток, откуда в желудочно- кишечный тракт, работая против внутренних паразитов.• Пирипроксифен нарушает развитие яиц и личинок блох.Дана Ультра Ошейник для собак крупных пород – специальный ошейник для защиты животного от наружных паразитов. Также такие ошейники еще называют «противоблошиными ошейниками».Несколько фактов об ошейнике Дана Ультра в цифрах:действует против 60 видов блох, которые переносят 25 видов заболеваний:на срок до 5 месяцев ошейник защитит вашего питомца от блох, вшей, власоедов;на срок до 4 месяцев – от клещей.А еще!Удобная застежка обезопасит ошейник от потери.Активные вещества выделяются с ошейника постепенно, не вызывая ожогов, и сохраняя действие на весь заявленный срок.При использовании ошейника имеющиеся личинки паразитов перестают расти и развиваться.Входящие в состав спрея активные компоненты действуют на очень широкий спектр насекомых.Также обеспечивает дополнительную профилактику глистов.

GENERAL INFORMATION 1.1 FORTIPAN (FORTIPAN) is a feed additive for the regulation of metabolic and physiological processes, strengthening the skeletal system in poultry. 1.2 FORTIPAN is a mixture of vitamins, amino acids, macro and microelements. As an active ingredient, 1000 ml contains: vitamin D3 - 200,000 ME, vitamin K1 - 350 mg, vitamin H (biotin) - 20 mg, L-histidine - 2000 mg, zinc - 10000 mg, manganese - 5000 mg , magnesium - 800 mg. The feed additive does not contain genetically modified products 1.3 In appearance FORTIPAN is an opaque opalescent liquid from light yellow to dark yellow, well soluble in water. 1.4 FORTIPAN is packaged in canisters made of polymer materials, sealed with screw caps of 1 and 10 liters, as well as in glass bottles of 100 ml. Store in closed packaging in a dry place protected from direct sunlight at a temperature from + 5C to + 25C. Shelf life in original packaging and subject to temperature conditions is 18 months. 1.5 Do not use the feed additive after the expiration date. ORDER OF USE Fortipan is used for regulation of metabolic and physiological processes of the skeletal system in poultry. Fortipan is administered orally with water for drinking daily for 5-7 days at the rate of: poultry: 100-200 ml per 100 liters of drinking water per day. The working solution is prepared immediately before use, taking into account the daily fluid intake and the required concentration. Do not use FORTIPAN in the drinking system together with oral vaccines, organic acids. The feed additive contains vitamins and amino acids for which there is no waiting period, that is, products from farm animals and poultry can be used for food purposes without restrictions. PERSONAL PREVENTION MEASURES When working with a feed additive, it is necessary to Imo observe the rules of personal hygiene and safety. The feed additive should be kept out of the reach of children. FULL NAME OF MANUFACTURER Manufacturer: CHEMIFARMA SpA, Italy Forli, st. Via Don Eugenio Servadei 16-47100

PHARMACOLOGICAL PROPERTIES The active ingredients of the drug "THIAM-OXY" are anti-biotics tiamulin and oxytetracycline, showing a synergistic effect when acting on pathogens of infectious diseases. The mechanism of action of this combination is that both antibiotic molecules block the same metabolic pathways, that is, the synthesis of bacterial protein by acting at the level of the 50S ribosomal subunit for tiamulin and the 30S and 50S subunits for oxytetracycline. Thiam-oxy has a broad spectrum of antimicrobial action. The drug is active against Brachyspira hyodysenteriae, Brachyspira pilosicoli, Mycoplasma spp., E. coli, Salmonella spp., Lawsonia intracellularis, Clostridium perfringens, Campylobacter coli, Streptococcus spp., Staphylococcus Borchino spp., Pasilteuretella spp., Pasilteuretella spp. , Erysipelothrix rushiopatiae, Haemophilus pleuropneumoniae, Chlamydia spp .. Listeria monocito-genes, Klebsiella pneumoniae and some others. After psroral administration of the drug, active substances are absorbed from the gastrointestinal tract and reach a maximum concentration in the blood serum after 2-4 hours, and then are distributed in the tissues of the body. Thiamulin is largely retained in the tissues of the lungs and colon, the highest levels of tetracyclines are found in the kidneys, liver and bones. The oral bioavailability of tiamulin reaches 90%. Oxytetracycline is absorbed mainly in the stomach and small intestine (up to 60%). In the gastrointestinal tract, tetracyclines can bind with bivalent metals (Ca, Fe, Cu, Co, Zn, Mn), antacids and dairy products, thus forming chelate compounds that are not absorbed and excreted in feces. The bioavailability of tetracyclines increases when given to animals on an empty stomach. Most of tiamulin (60-65%) through bile is excreted from the body with feces, 30-35% - with urine. Oxytetracycline is excreted through the kidneys in the urine unchanged or in the form of metabolites, about 10% - with feces. PROCEDURE FOR USE OF THE PREPARATION Thiam-oxy is used for medicinal purposes in pigs for dysentery , mycoplasma bronchopneumonia, infectious atrophic rhinitis, edema disease, colibacteriosis. salmonellosis, actinobacillary pleuropneumonia, hemophilia and other diseases caused by microorganisms sensitive to tiamulin and oxytetracycline. The drug is administered to pigs as part of a medicinal feed at a dose of 300-500 g per 100 kg of feed for 5 days (which corresponds to a dose: 6.0 mg of tiamulin and 45.0 mg of oxytetracycline per 1.0 kg of animal body weight in day). The medicinal food with the preparation is placed in feeders cleaned of unused food residues as the only source of nutrition. After carrying out the recommended period of treatment, the feeders are filled with the usual compound feed. It is not recommended to use the drug in conjunction with ionophore antibiotics: monensin, narasin, salinomycin and lasalocide, as well as simultaneously with milk and dairy products, calcium, magnesium, zinc, iron preparations , copper, cobalt. Do not administer to animals with hypersensitivity to tetracyclines, thiamulin and renal failure. 3.4 During the treatment period in some pigs, side effects are possible in the form of skin erythema and superinfection caused by microorganisms resistant to tiamulin. 3.5 Slaughter of animals for meat is allowed 30 days after the end of the preparation. In case of forced slaughter of animals earlier than the specified time, meat and internal organs are used as feed for carnivores. PERSONAL PREVENTION MEASURES All work with the drug is recommended to be carried out in overalls with the use of personal protective equipment observing safety regulations. Do not smoke, drink or eat while working. It is forbidden to work with the drug for persons with hypersensitivity to tiamulin and tetracyclines. PROCEDURE FOR SUBMITTING CLAIMS In case of complications after using the drug, its use is stopped, the consumer applies to the state veterinary institution on the territory of which he is located. Veterinary specialists of this institution study compliance with all rules for using the drug in accordance with the instructions. When a negative effect of the drug on the animal's body is revealed, veterinary specialists take samples in the required amount for laboratory tests, draw up a sampling report and send it to the State Institution "Belarusian State Veterinary Center" for confirmation of compliance with regulatory documents.

GENERAL INFORMATION Sanajod. Sanayod is a light red to dark brown liquid. 1.0 ml of Sanayod contains 0.023 g of active iodine and 0.065 g of phosphoric acid as an auxiliary substance, solvent up to 1.0 ml. The drug is produced in polymer cans of 1.0 l, 5.0 l and 10.0 l. DISINFECTING PROPERTIES Saniod is a disinfectant with a broad spectrum of action, has antimicrobial, antifungal, anti-inflammatory and astringent action. The ability of iodine to exhibit disinfecting properties is associated with the ability to replace covalently bound hydrogen in compounds containing functional groups. Phosphoric acid provides the required pH for the preparation. The active forms of iodine are polarized by water, enter into an electrophilic interaction with the enzymes of the respiratory chain (blocking the transport of electrons), as well as with amino acids that make up the proteins of the cell membrane located in the cell wall. As a result, the stabilized tertiary structure of the protein, which is required to maintain the respiratory chain, is destroyed, which leads to irreversible damage to microorganisms. The drug belongs to the 3rd group of toxic compounds. Sanayod solutions do not have an irritating effect, do not cause corrosion of metals. ORDER OF APPLICATION OF THE PREPARATION Sanayod is used for preventive and forced (current and final) disinfection of livestock, poultry and fur-breeding premises, incubators , premises for the slaughter of animals, animal care products, equipment, vehicles used to transport animals and raw materials of animal origin. Disinfection is carried out after thorough mechanical cleaning and washing of the treated surfaces. Working solutions of the drug are prepared in a clean glass or polymer material by diluting the product with water at a temperature of 20-25 ° C. Disinfection in the absence of animals by irrigation. For prophylactic and forced disinfection in cases of infections of bacterial, viral and fungal etiology, the causative agents of which, in terms of resistance to disinfectants, belong to group 1 (unstable) and 2 (resistant), as well as for disinfection of premises for slaughtering animals, incubators, premises for milk processing, milking parlors, transport for transporting animals, use 0.25% - 0.6% working solution of Sanayod (250 - 600 ml of the drug per 100 liters of water), at a consumption rate of 0.3 l / m2 of the treated surface. PERSONAL PREVENTION MEASURES Persons who are at least 18 years old, pregnant women and persons who have contraindications for working with disinfectants are allowed to work with Sanayod. When working with the drug, you must follow the generally accepted measures. All types of work are carried out using personal protective equipment. After finishing work, wash hands and face thoroughly with soap and water. When working with a concentrated drug, rubber gloves should be used. PROCEDURE FOR SUBMISSION OF CLAIMS In case of complications after using the drug, its use is stopped and the consumer contacts the State Veterinary Institution, on the territory of which he is located. Veterinary specialists of this institution study compliance with all rules for the use of the drug in accordance with the instructions. Upon confirmation of the detection of a negative effect of the drug on the animal's body or non-compliance of the drug in appearance, veterinary specialists take samples in the required amount for laboratory tests, draw up a sampling report and send it to the State Institution "Belarusian State Veterinary Center" (Minsk, st. Krasnaya, 19a) to confirm the compliance of the drug with regulatory documentation. FULL NAME OF MANUFACTURER CHEMIFARMA SpA, Italy, Forlì, st. Via Don Eugenio Servadei, 16- 47100.

GENERAL INFORMATION. < p>1.1 PANTOSAL NEW is a feed additive containing water-soluble micro and macronutrients for farm animals and poultry. In 1000 ml of the supplement contains: manganese -12500 mg, copper-3500 mg, zinc-7000 mg, calcium-30,000 mg and phosphorus-30,000 mg filler-purified water-up to 1000 ml. The feed additive does not contain genetically engineered products. < p>1.2 In appearance, PANTOSAL NEW is a clear liquid from light green to dark green in color, well soluble in water. < p>1.3 PANTOSAL NEW is packaged in cans made of polymer materials, capped with screw-on lids, of 1 and 10 liters each. Each package is marked in Russian with the following information: the manufacturer's organization, its address and trademark, the name of the feed additive, purpose, method of use, composition and guaranteed indicators, batch number, volume, date of manufacture, term and storage conditions, marked "For animals" < p>1.4 Stored in a closed package in a dry place, protected from direct sunlight, at a temperature of +5C to +25C. The shelf life in the original packaging and in compliance with the temperature regime is 18 months. < p>1.5 Do not use the feed additive PANTOSAL NEW after the expiration date.BIOLOGICAL PROPERTIES2.1 MANGANESE contained in a readily available form of organic salts, the processes involved in the assimilation of calcium and phosphorus affects the growth of young, productive adults through participation aktivacii sootvetstvuyuschih enzymes. It participates in the regulation of the functions of the nervous system of fat and carbohydrate metabolism.COPPER, which is contained in an easily accessible form in the form of organic salt, participates in the processes of hematopoiesis, is part of enzymes, increases the body's resistance to infections, and has bacteriological effects. < p>ZINC, which is contained in an easily accessible form as an organic salt, is part of numerous enzyme systems that stimulate the exchange of proteins and carbohydrates, which have a direct impact on the growth and development of animals and birds. It affects the reproductive ability. Zinc is involved in the development of the backbone, plays a significant role in the processes of tissue respiration, and supports the acid-base balance of the body. < p>CALCIUM, which is contained in an easily accessible form, serves in the body as a material for building bone tissue. It takes part in the processes of excitability of muscle and nervous tissue, activation of enzymes and hormones, and creation of bioelectric potential. It is necessary for the body in the processes of blood clotting. < p>PHOSPHORUS, contained in an easily accessible form, plays an important role in the construction of the skeleton, carbohydrate metabolism, takes part in fat metabolism, while fatty acids, entering the blood, combine with phosphoric acid and choline, forming lecithin. Phosphorus is part of the nucleic acids that make up the nuclear substance of all cells in the body. < p>2.2 The feed additive provides the body with an optimal amount of basic macro and microelements that have not only a catalytic function, but also act as part of enzymes or simple catalysts for the activity of enzymes. In addition, macro and microelements have a protective effect on the body. < p>APPLICATION PROCEDUREPantosal new < / strong> is used to improve metabolism and enrich the diets of farm animals and birds with macro and microelements in an easily digestible form. The use of feed additives is recommended in stressful situations.The feed additive is used orally with water for drinking daily for 5-7 days at the rate of: < strong>poultry: < / strong> 50-100 ml per 100 liters of drinking waterlarge animals: < /strong>(cattle, pigs, horses) 30 ml per head < strong>small animals: (sheep, goats, piglets, calves and foals) 10 ml per head.If necessary, repeat after a week.The working solution is prepared immediately before use, taking into account the daily consumption of liquid and the required concentration.Complications and side effects when using the feed additive in accordance with these instructions for use were not detected.Do not apply Pantanal was NEW in the drinking system in conjunction with vaccines oral application of organic acids.The feed additive contains macro and microelements, for which there is no waiting period, that is, products from farm animals and poultry can be used for food purposes without restrictions.PERSONAL PREVENTION MEASURESWhen working with a feed additive, it is necessary to observe the rules of personal hygiene and safety. In case of accidental contact with the skin or mucous membranes, wash them with plenty of water. If necessary, consult a doctor. Have PANDASAL NEW slideout to store in the places inaccessible for children. < p>THE PROCEDURE FOR FILING COMPLAINTS.In case of discrepancy was PANTANAL NEW requirements of this manual, as well as the detection of complications, the use of feed additives and stop misleading GU "Belgosvettsentr" (Minsk, ul. 19a, tel - 2904279), and you must pass 3 samples from the party, which identified complications.FULL NAME OF THE MANUFACTURER.Manufacturer: CHEMIFARMA S. p. A., Italy, Forli, Via Don Eugenio Servadei, 16-47100 < /p>

< h2>Oxytetra 50% W. S.For the treatment and prevention of diseasesof bacterial etiology in farm birdsGeneral informationTrade name of the drug: Oxytetra 50% W. S. (Oxytetra 50% W. S.).International nonproprietary name: oxytetracycline.Dosage form: powder for oral administration.Oxytetra 50% W. S. in 1 g contains as the active substance oxytetracycline hydrochloride - 500 mg, and as an auxiliary substance lactose – up to 1 g.In appearance, the Occiteter is 50% W. S. it is a light yellow powder; it is easily soluble in water.Oxytetra 50% W. S. they are produced packaged in 0.1 and 1 kg packages in hermetically sealed laminated bags of the appropriate capacity.Store the drug in the closed packaging of the manufacturer in a dry, protected from light place, separate from food and feed, at a temperature of 5 0C to 20 0C.The shelf life of the drug under the conditions of storage in a closed package is 2 years from the date of production, after opening the package-28 days.< br>It is forbidden to use the drug after the expiration date.Oxytetra 50% W. S. keep out of the reach of children.Unused medicinal product is disposed of in accordance with the requirements of the legislation.Pharmacological propertiesOxytetra 50% W. S. it belongs to the antibacterial drugs of the tetracycline group.Oxytetracycline hydrochloride, which is part of the drug, has a wide spectrum of antibacterial action, inhibits the growth and development of most Gram-positive and Gram-negative microorganisms, including streptococci, staphylococci, Escherichia, Salmonella, pasteurella, Clostridium, actinobacteria, as well as some types of mycoplasma, rickettsia, chlamydia and protozoa.The mechanism of bacteriostatic action is based on the suppression of microbial cell protein synthesis (blockade of ribosome function) and blockade of RNA synthesis.After oral administration of the drug, oxytetracycline is well absorbed in the gastrointestinal tract, penetrates into most organs and tissues, reaching a maximum concentration in the blood after 1-1. 5 hours, and is kept at the therapeutic level for 10-12 hours after administration. The antibiotic is excreted from the body mainly in unchanged form with bile and urine.Oxytetra 50% W. S. according to the degree of exposure to the body, it belongs to moderately dangerous substances (hazard class 3 according to GOST 12.1.007).Application procedureOxytetra 50% W. S. is prescribed to broiler chickens and repair young birds for therapeutic and prophylactic purposes for respiratory infections and diseases of the gastrointestinal tract of bacterial etiology caused by pathogens sensitive to tetracyclines.It is forbidden to use the drug to laying hens and repair young chickens older than 16 weeks of age, due to its accumulation in eggs.Oxytetra 50% W. S. apply to birds orally individually or in a group way with water for drinking in a daily dose of 60 g per 100 liters of drinking water for 3-5 days.The therapeutic solution is prepared daily based on the daily water requirements of birds.During the treatment period, the therapeutic solution should be the only source of drinking water.In the case of an overdose of the drug, it is possible to reduce the consumption of poultry feed and water, reduce weight gain. In these cases, general measures are used to eliminate the drug from the body.The features of the drug's action during its first use and cancellation were not revealed.You should avoid skipping the next dose of the drug, as this can lead to a decrease in its therapeutic effectiveness. In case of missing one dose, the use of the drug is resumed in the same dosage and according to the same scheme.When using an Oxytetre of 50% W. S. in accordance with these instructions, side effects and complications in birds, as a rule, are not observed.< br>Oxytetra 50% W. S. should not be used together with bactericidal antibiotics, kaolin, preparations and feed additives containing iron, magnesium, calcium and aluminum, due to a pronounced decrease in the antibacterial effect of the drug.Slaughter of birds for meat is allowed no earlier than 15 days after the last application of Oxytetra 50% W. S. The meat of birds that were forcibly killed before the deadline can be used as food for fur-bearing animals.Personal prevention measuresAll work with Oxytetra 50% W. S. must be carried out with the use of protective clothing and personal protective equipment (rubber gloves, safety glasses, respirator).It is forbidden to drink, smoke or eat while working. At the end of the work, wash your face and hands thoroughly with soap and rinse your mouth with water.In case of accidental contact of the drug with the skin or mucous membranes of the eye, they should be washed with plenty of water. People with hypersensitivity to the components of the drug should avoid direct contact with Oxytetra 50% W. S. In case of allergic reactions or accidental ingestion of the drug in the human body, you should immediately contact a medical institution (have the instructions for use of the drug or the label).Empty bags from under the drug may not be used for household purposes, they are subject to disposal with household waste.Manufacturer< / h3> "CEVA Sante Animale"; La Ballastiere-B. P. 126, 33501 Libourne Cedex, France.

Multivit + Minerals maintains and corrects the vitamin and mineral balance and the required level of substances with an antioxidant effect. Effective complex action is ensured due to the presence in its composition of a balanced composition of biologically available ingredients with synergistic properties. Multivit + Minerals "is used for the treatment and prevention of diseases of animals, including fur animals and birds, associated with a lack of vitamins and microelements. It is recommended to use with high productivity of farm animals, intensive loads, unbalanced diet, stress, including before transportation, during convalescence, especially after chemotherapy, to normalize the function of the reproductive organs, as well as in preparation for routine vaccination and deworming. The drug is administered to animals intramuscularly once or twice with an interval of 10-14 days. b the contents of the bottle to a temperature of at least 20 ° C. Approximate doses for different species of animals are presented in the table: Type of animal < / p> Dose, cm / kg Cattle, horses 2.0 -6.0 cm3 / 100 kg of live weight Sheep, goats, pigs 1.5-2.5 cm3 / 50 kg of live weight Piglets, kids, lambs 1.0-1.5 cm3 / 10 kg live weight Dogs, fur animals 0.5 - 1.0 cm3 / 10 kg of live weight < p> Do not use the medicinal product for felines and newborns in the first week of life due to the content of benzyl alcohol! The bird "Multivit + Minerals" is administered orally with water for drinking in doses: Type of animal Dose, cm3 / 10 head Chickens 2.0 cm3 Chickens 1.0 cm 3 Turkey 5.0 cm3 < / tr> Turkey poults 2.0 cm3 < p> Geese 6.0 cm3 Ducks 4.0 cm3 Goose and ducklings 3 , 0 cm3 Pigeons 1.5 cm3 For exotic birds, the drug is administered for prophylactic purposes at a dose of 6 drops / l of water for drinking, and for medicinal ones - 12-16 drops / l of water for drinking for 2 -3 days. Re-administration of the drug is possible only after 2-3 months. Subject to the recommendations of this instruction, side effects and complications were not identified.

The drug is used for the treatment and prevention of mastitis, abscesses, acute and chronic arthritis, bursitis, tevdinitis, articular and muscular rheumatism, osteochondrosis. lumbago, lymphadenitis, bruises. Mastissept is applied daily (2-3 times a day), in a thick layer on the skin in the area of ​​the pathological process, followed by intensive rubbing in. With mastitis, massage the udder. The duration of treatment is on average 3-4 days When using the ointment, side effects are not noted, and does not require the use of any protective equipment by the Staff. Due to the irritating effect, do not apply the drug is open wounds, erosive surfaces and mucous membranes. Meat and milk from treated animals are allowed to be used in food for people not earlier than three days after the last use of the drug. Until the end of this period, milk and meat can be used as feed for carnivores.

GENERAL INFORMATION. 1.1 METAPHYSIOL is a feed additive for the regulation of metabolic and physiological processes in the liver of farm animals and poultry. 2.2 METAFIZIOL is a multicomponent mixture of fat and water-soluble vitamins and amino acids , antioxidant and stabilizer. As an active ingredient, 1000 ml contains: L-carnitine - 5000 mg, vitamin B6-500 mg, vitamin B12-15 mg, nicotinamide - 150 mg, calcium pantetonade (D-panthenol) -1000 mg. DL-methionine -10000 mg, sorbitol-100 mg L-lysine - 1000 mg, L-glycine 2000 mg, L-glutamic acid - 1500 mg, L-aspartic acid - 1500 mg. The feed additive is not contains genetically modified products. 1.3 In appearance, METAFIZIOL is a transparent liquid from light red to dark red, well soluble in water. 1.4 Feed additive is packaged in canisters made of polymeric materials, sealed with screw caps of 1 and 10 liters, as well as in glass bottles of 100 ml. Each package is marked in Russian, indicating: the manufacturer's organization, its address and trademark, the name of the feed additive, purpose, method of application, composition and guaranteed parameters, batch number, volume, date of manufacture, shelf life and storage conditions, marked "For animals ". Store in a closed container in a dry place, protected from direct sunlight, at temperatures from + 5C to + 25C. Shelf life in original packaging and subject to temperature conditions - 18 months. 1.5 Do not use METAFIZIOL after the expiration date. APPLICATION PROCEDURE. METAFIZIOL provides detoxifying effect in farm animals and poultry, increases energy capacity, eliminates the toxic effect of ammonia during the period of intensive growth, performs choleretic and vitaminizing actions. The feed additive is used orally with water for drinking daily for 5-7 days at the rate of: poultry: 50-100 ml per 100 liters of drinking water large animals: (cattle, pigs, horses) 30 ml per head small animals: (sheep, goats, piglets, calves and foals) 10 ml per head. Repeat if necessary after a week. < / p> The working solution is prepared immediately before use, taking into account the daily fluid intake and the required concentration. Complications and side effects during use no feed additive has been identified in accordance with this instruction. Do not use METAFIZIOL in the drinking system together with oral vaccines, organic acids. The feed additive contains vitamins and amino acids for which there is no period expectations, i.e. products from farm animals and poultry can be used for food purposes without restrictions. PERSONAL PREVENTION MEASURES. When working with a feed additive, you must follow the rules of personal hygiene and technology security. In case of accidental contact of the product on the skin or mucous membranes, wash them with plenty of water and, if necessary, consult a doctor. METAFIZIOL should be stored in places inaccessible to children. PROCEDURE FOR SUBMISSION OF CLAIMS. In case of non-compliance of the feed additive with the requirements of this instruction, as well as detection of complications, the use of the feed additive is discontinued and the State Enterprise "Belgostsvettsentr" "(Minsk, Krasnaya str. 19a, tel. 2904279), and it is also necessary to transfer 3 arrivals of the additive from the batch in which complications were detected. FULL NAME OF THE MANUFACTURER. Manufacturer: Chemifarma SpA, Italy, Forlì, st. Via Don Eugenio Servadei 16-4710011а1

1. GENERAL INFORMATION< / p> < p>1.1 "Lauritin-C" (Lauritinum C) < p>1.2 The drug is a sterile, transparent, colorless or light yellow liquid with a specific smell of camphor. < p>1.3 The main active ingredients are contained in 1.0 cm3 of the preparation: ascorbic acid-10.0 mg; camphor-1.0 mg; butaphosphane-32.0 mg and excipients-glucose monohydrate-110.0 mg; magnesium chloride-0.13 mg; calcium chloride-0.9 mg / ml; magnesium sulfate-0.08 mg; neutral ingredients: - stabilizers, preservatives and water for injection. < p>1.4 "Lauritin-C" is produced in glass or polypropylene transparent bottles of 100 cm3. < p>1.5 The drug is stored in its original packaging according to list B, in a dry, protected from light place at a temperature of + 8 to + 15 °C. It is allowed to transport "Lauritin-C" packed in an isothermal container for 7 days at an ambient temperature from -20 to + 30 °C. 1.6 The shelf life of the drug is 2 (two) years from the date of manufacture, subject to the storage rules.2. PHARMACOLOGICAL PROPERTIES< / strong>2.1. "Lauritin-C" has a pacemaker, analeptic, antihistamine, antiaggregate and antioxidant effects on the animal's body due to the presence of a balanced composition of biologically available ingredients in its composition. It stimulates the restoration of the general resistance of the body by stabilizing its hormonal background, correcting the functions of the endocrine glands, energy metabolism and metabolism in general. Ascorbic acid is an antioxidant, participates in the formation of collagen, the synthesis of corticosteroids, serotonin, interferon, in the process of immunomodulation, increasing the body's resistance to infections. Promotes phagocytosis, blood clotting, tissue regeneration, reduces vascular permeability, reduces the need for vitamins B, B2, A, E, folic acid, pantothenic acid. It has antiaggregate properties. Maintains the colloidal state of the intercellular substance, normalizing capillary permeability and blood microcirculation. Activates proteolytic enzymes, participates in the exchange of aromatic amino acids, pigments and cholesterol, promotes the accumulation of glycogen in the liver. It is mainly metabolized in the liver to deoxyascorbic acid and then to oxalic acid and diketogulonic acid. It is excreted through the kidneys, intestines, with sweat and milk, in the form of unchanged ascorbate and metabolites. Camphor, stimulating the central nervous system, has a stimulating effect on blood circulation, respiration and metabolic processes in the myocardium. With the weakening of the tissue respiration of the myocardium, it normalizes the oxidative processes, increasing the metabolism and increasing the sensitivity of the heart muscles to the influence of sympathetic nerves. Camphor tones the heart well: - during tachycardia, the heart rate slows down while increasing the contraction of a single push. The release of camphor from the body occurs by its diffusion into the blood of regional microcapillaries. It is excreted through the kidneys, lungs and with bile for 2-3 days in an unchanged form. Butaphosphane, which is part of the drug, has a stimulating effect on most metabolic processes in the body, increases the tone of smooth muscles, myocardium, and improves bone regeneration. It stimulates and normalizes metabolic and energy metabolism, improves the utilization of glucose in the blood, accelerates the metabolic processes by stimulating the ADP-ATP cycle, and protein synthesis. It is not deposited in organs and tissues and does not penetrate into milk. It is excreted from the body through the kidneys.3. PROCEDURE FOR THE USE OF THE DRUG< / p> < p>3.1 "Lauritin-C" is used for all types of productive and non-productive animals. It is an effective tool in the intensive care of critical conditions (shock) with multiple organ failure. In the treatment of various diseases associated with the suppression of respiratory, cardiovascular and hepatic-renal activity of the body, acute and chronic intoxication, including infectious diseases accompanied by fever. Dilutes sputum, helping to improve ventilation in the pulmonary system. By stabilizing hormones and energy metabolism, effective in disorders of metabolism and activation of the General resistance of the organism to reduce the recovery time after an illness, a difficult birth, hyperresponsiveness, stress factors, etc. Used for sedation in the post anesthetic period. < p>3.2 "Lauritin-C" is administered intravenously, intramuscularly or subcutaneously 1-2 times a day. To Enter Slowly! < p>3.3 The dosage and duration of use is determined by the veterinarian individually, depending on the condition of the animal. Average doses: K R S, horses-10-20 ml per animal; foals, calves - 5-10 ml per animal; pigs, sheep, goats-2-5 ml; dogs, cats-1.0 -5.0 ml per animal; rabbits, minks-0.2 -0.5 ml per animal. The drug is not toxic. If necessary, the dose can be doubled. It is allowed to use it daily until the animal is fully recovered. < p>3.4 Side effects: with caution, it should be used in females during pregnancy and lactation. A single passing vomiting is possible with a jet intravenous injection. Intramuscular and subcutaneous jet injection causes a painful reaction. < p>3.5 Do not mix with other drugs in the same syringe. It is permissible to mix with neutral liquids during infusion therapy. 3.6 Slaughter of large, small cattle and pigs for meat is allowed no earlier than 3 days after the last use of the drug. Milk of dairy cows and sheep is allowed to be used no earlier than 3 days after the last application of the drug. The meat of animals forcibly killed before the expiration of the specified period can be used as food for fur-bearing animals.4. PERSONAL PREVENTION MEASURES < p>4.1 When working with the drug, it is necessary to observe generally accepted personal hygiene and safety measures5. THE PROCEDURE FOR FILING COMPLAINTS< / p>5.1 In the event of complications after the use of the drug, its use is discontinued, the consumer applies to the State Veterinary Institution in the territory where he is located. Veterinary specialists of this institution study compliance with all the rules for the use of this drug in accordance with the instructions. When confirming the detection of a negative effect of the drug on the animal's body, veterinary specialists take samples in the required amount for laboratory tests, write a sampling report and send it to the State Institution "Belarusian State Veterinary Center" of the Republic of Belarus, Minsk, Krasnaya str.19a for confirmation of compliance with regulatory documents.6. FULL NAME OF THE MANUFACTURER< / strong>6.1 " ImmKont GmbH "(Germany), Angermunder str. 45, Eberswalde D -16227, Germany. Telefax +49 3334 383075; e-mail: The manual was developed by the specialists of the company "ImmKont GmbH" (Germany)

GENERAL INFORMATION The drug is intended for the treatment of calves, pigs, chickens, turkeys, rabbits, laying hens INDICATIONS: Bacterial enteritis from gram-negative bacteria such as Salmonella, E. coli, Hemophilus influenzae, Pasteurella spp., Klebsiella spp., Shigella, Pseudomonas, Enterobacter spp. E Proteus spp. Dosage and method of administration In drinking water or liquid feed for all types of animals: 4.2 - 5.0 ml / 100 kg of animal weight (equal to 5.0 - 6.0 mg of colistin sulfate / kg of animal weight) depending on age, weight and water consumption of animals, 3-15 days. To ensure the correct dosage, the weight of the animal must be determined as accurately as possible to avoid treatment with insufficient doses. Use proper and appropriate dispensing equipment. Do not use in solid feed. For correct use, remove residual water or liquid feed from the drinking bowls and use Colisid according to your veterinarian's instructions. It is recommended to inject the product every 12 hours, dividing the daily dose into two applications. At the end of the treatment, restore drinking water without the drug. Ingestion of the drug can be changed depending on the disease. Repeated or prolonged use should be avoided by improving containment and disinfection practices. SPECIAL PRECAUTIONS The use of veterinary drug (colistin) in poultry must comply with Commission Regulation EC 1177/2006 and national regulations transposition. Due to possible variations (in place and time) in the sensitivity of the target species to colistin, a bacteriological examination and susceptibility test are recommended. Any use of the drug not in accordance with the instructions can increase the prevalence of bacteria resistant to colistin and can reduce the effectiveness of treatment with other antibiotics of the polymyxin group and develop cross-resistance. Do not leave water diluted with the preparation within reach of other animals. Special precautions must be taken by the person using the drug when treating animals: No special precautions are required when working with the drug. However, it is advisable to avoid direct skin contact and inhalation of the drug. The use of protective gloves is recommended when working with the drug. In case of accidental contact, wash thoroughly with soap and water. If irritation persists, seek medical attention. People with known hypersensitivity to colistin should avoid contact with veterinary medicinal products. CONTRAINDICATIONS Do not use in animals with known hypersensitivity to colistin. Do not use in animals with a polygastric digestive system with functioning scars. ADVERSE REACTIONS Prolonged use of the drug can cause intestinal dysbiosis and lead to the development of insensitive microorganisms. In case of any adverse reactions or other reactions not mentioned here, please notify your veterinarian.

Composition and form of releaseInotyl 200 contains 200 mg of tylosin tartrate as the active ingredient in 1 ml, and benzyl alcohol, dimethylacetamide, propylene glycol, and water for injection as excipients.Inotil 200 is produced packaged in 100 ml glass bottles of the appropriate capacity, capped with rubber stoppers, reinforced with aluminum caps. The vials are packed in individual cardboard boxes. The drug in appearance is a transparent, colorless, oily liquid.Pharmacological propertiesIntel 200 (200 Inotyl) - an antibacterial drug in the form of a solution for injection, intended for the treatment of animals with diseases of bacterial etiology.Tylosin tartrate, which is part of the drug, belongs to the macrolide group of antibiotics, is active against most Gram-positive and some Gram-negative microorganisms, including Stapylococcus spp., Streptococcus spp., Clostridium spp., Corynebacterium spp., Pasteurella spp., Treponema hyodysenteriae, Chlamydia spp., Spirocheta spp. and Mycoplasma spp. Microorganisms of the Enterobacteriaceae family are resistant to the antibiotic. The mechanism of bacteriostatic action of tylosin tartrate is to block protein synthesis in the microbial cell. When administered intramuscularly, the antibiotic is well absorbed from the injection site into the blood and penetrates almost all organs and tissues of the body. The highest levels of tylosin are found in the lungs, liver, mammary glands, and kidneys. After a single injection, the therapeutic concentration of the antibiotic remains in the body for at least 20 hours.Tylosin is released from the body of animals mainly with bile, in smaller amounts - with urine and milk.According to the degree of exposure to the body, Inotil 200 is a moderately dangerous substance (hazard class 3 according to GOST 12.1.007-76).Indications for useInotil 200 is used for the treatment of bronchopneumonia, infectious agalactia of large and small cattle, enzootic pneumonia, arthritis, dysentery, atrophic rhinitis and erysipelas of pigs, mastitis of cattle, as well as for therapeutic and prophylactic purposes in secondary infections. < h3>DosageThe drug is used intramuscularly in animals, 1 time a day for 3 days in the following doses: cattle-0.5-1 ml/20 kg of animal weight; sheep and pigs-1 ml/20 kg of animal weight.When using the drug to pigs, in rare cases, allergic reactions are possible, which quickly pass after stopping the administration of the drug. In connection with a possible pain reaction, do not inject more than 10 ml in one place to cattle, pigs and sheep more than 5 ml, and also mix it in one syringe with other medicines.Special instructionsSlaughter of animals for meat is allowed no earlier than 8 days after the last use of the drug. The meat of animals forcibly killed before the expiration of the specified period can be used for feeding fur-bearing animals.Milk of dairy animals during the treatment period within 4 days after the last administration of the drug is prohibited to be used for food purposes. Such milk after boiling can be used for feeding fur-bearing animals.Storage conditions and terms< / h3> < p>Store the drug in a closed package, in a dry place, protected from direct sunlight, at a temperature from 5 0C to 25 0C.The shelf life of the drug, subject to storage conditions, is 2 years from the date of manufacture.Inotil 200 should not be used after the expiration date.Intel 200 should be stored in places inaccessible to children.Manufacturer< / h3> "CEVA Sante Animale" / "CEVA Sante Animale" (France)

InoxelFor the treatment of diseases of bacterial etiology in cattle and pigs, prevention of bacterial infections in chickens < h3>General informationTrade name of the medicinal product: Inoxel.International nonproprietary name: ceftiofur.Dosage form: powder for the preparation of a solution for injection. Inoxel as an active substance in 1 bottle contains ceftiofur sodium-1.06 g (equivalent to 1 g of ceftiofur) or 4.2 g (equivalent to 4 g of ceftiofur).In appearance, the drug is an amorphous powder of white or light beige color.Inoxel is produced in the form of a sterile powder, packaged in 1.06 g or 4.2 g in glass vials with a capacity of 20 ml or 80 ml, respectively. The powder bottles are packed in individual cardboard boxes.Store Inoxel in the closed packaging of the manufacturer, separately from food and feed, in a dry place, protected from direct sunlight, at a temperature of 5 0C to 20 0C. The shelf life of the drug under the conditions of storage in a closed package is 2 years from the date of production, after opening the bottle – 28 days < br>It is forbidden to use Inoxel after the expiration date. Inoxel should be stored out of the reach of children.Unused medicinal product is disposed of in accordance with the requirements of the legislation. Pharmacological propertiesInoxel belongs to the antibacterial drugs of the cephalosporin group.Ceftiofur sodium, which is part of the drug, has a wide spectrum of antibacterial action on Gram-negative and gram-positive bacteria, including strains that produce beta-lactamase, and some anaerobic bacteria, including: Escherichia coli, Pasteurella (Mannheimia) haemolytica, Pasteurella multocida, Haemophilus somnus, Actinobacillus pleuropneumoniae, Haemophilus parasuis, Salmonella cholerasuis, Salmonells typhimurium, Streptococcus suis, Streptococcus zooepidemicus, Streptococcus equi, Streptococcus agalactiae, Streptococcus dysgalactiae, Streptococcus bovis, Pasteurella spp., Staphilococcus spp., Actynomyces pyogenes, Klebsiela, Citrobacter, Enterobacter, Bacillus spp., Proteus spp., Fusobacterium necrophorum and Porphiromonas assacharolytica (Bacteroides melaninogenicus). The mechanism of the bactericidal action of the antibiotic is to inhibit the synthesis of the cell wall of the bacterium. After parenteral administration, ceftiofur enters the systemic bloodstream, is rapidly metabolized, reversibly binds to plasma proteins, and is concentrated at the sites of inflammation.The maximum concentration of the antibiotic in the blood plasma after intramuscular administration of the drug is reached in 0.5-2 hours and remains at the therapeutic level for up to 24 hours. The antibiotic is excreted from the body mainly in the urine and partially with feces, the half-life, depending on the type, age of the animal and the method of administration, is 10-19 hours.< br> Inoxel by the degree of exposure to the animal body belongs to the moderately dangerous substances (hazard class 3 according to GOST 12.1.007). Application procedureInoxel is prescribed for the treatment of bacterial respiratory infections in cattle caused by Pasteurella haemolytica, Pasteurella multocida, Haemophillus somnus, Actinobacillus pleuropneumoniae, and pigs caused by Pasteurella haemolytica, Pasteurella multocida, Haemophillus somnus, Actinobacillus pleuropneumoniae, Salmonella cholerasuis, Streptococcus suis; for the treatment of necrobacteriosis associated with Fusobacterium necrophorum and Porphiromonas assacharolytica (Bacteroides melaninogenicus in cattle, and for the prevention of early death of one-day-old chickens caused by Escherichia coli and Staphylococcus aureus. Contraindication to the use of Inoxel is an increased individual sensitivity of the animal to antibiotics of the cephalosporin group.Inoksel used for animals parenterally in a sterile solution, making the vial 1.06 g sterile powder make 20 ml of solvent (water for injection, saline diluent for vaccines Marek (if the drug is used to treat birds)), in a bottle from 4.02 g of sterile powder 80 ml of solvent. Dissolution Inoksela should be carried out as quickly as possible, water for injection (water for injection, saline diluent for vaccines Marek (if the drug is used to treat birds)), type in a sterile syringe with a large amount of needle with a large diameter and contribute to the vial with powder, then shake the vial immediately until the powder is completely dissolved. The resulting therapeutic solution contains 50 mg of ceftiofur /ml. The term of use of the therapeutic solution is: when stored in a dark place at a temperature of 5°C to 20°C – 12 hours, when stored in the refrigerator at a temperature of 2°C to 8°C-7 days, when stored in frozen form at a temperature of minus 4 ° C to minus 18°C-8 weeks.The therapeutic solution is administered to the animal once a day in the following doses: - to cattle-intramuscularly 1 ml per 50 kg of weight (1 mg of ceftiofur per 1 kg of animal weight). The course of treatment for respiratory diseases caused by Mannheimia haemolytica, Pasteurella multocida and Histophilus somni – 3-5 days; for acute interdigital necrobacillosis (panaritium, hoof rot) caused by Fusobacterium necrophorum and Bacteroides melaninogenicus – 3 days; - pigs – intramuscularly 1 ml per 16 kg of weight (3 mg ceftiofura per 1 kg of animal weight). The course of treatment for respiratory diseases caused by Pasteurella multocida, Actinobacillus pleuropneumonia and Streptococcus suis is 3-5 days; - one-day-old chickens-subcutaneously in the neck at a dose of 0.2 ml. Before administration to chickens, the standard solution (50 mg of ceftiofur/ml) is diluted with water for injection in accordance with the table, so that 0.2 ml of the administered solution contains 0.08 – 0.2 mg of ceftiofur (3 column of the table).TableDose of ceftiofur/chicken Volume of standard Inoxel solution (50 mg / ml) Volume of added solvent1 2 30.08 mg 1 ml 124 ml < br>0.10 mg 1 ml 99 ml < br>0.12 mg 1 ml 82 ml0.14 mg 1 ml 70 ml0.16 mg 1 ml 61 ml0.18 mg 1 ml 54 ml0.20 mg 1 ml 49 mlWith an overdose of the drug, the animal may experience a decrease in appetite, inflammatory reaction at the injection site.Features of the action at the first administration of the drug and at its cancellation were not revealed.Skipping the next dose of the drug should be avoided, as this can lead to a decrease in therapeutic effectiveness. In case of missing one dose, it is necessary to introduce it as soon as possible, then the interval between injections of the drug does not change.Side effects and complications when using Inoxel in accordance with this instruction, as a rule, are not observed. In some animals, a local reaction may occur at the injection site in the form of edema, which resolves spontaneously within a few days. With increased individual sensitivity to the drug and the manifestation of allergic reactions, the use of the drug is discontinued and the animal is prescribed antihistamines and symptomatic therapy.Inoxel should not be prescribed simultaneously with drugs of bacteriostatic action, due to a decrease in its bactericidal activity, as well as mixed in one syringe with other drugs.Slaughter of cattle for meat is allowed no earlier than 24 hours, pigs-no earlier than 48 hours after the last application of Inoxel. The meat of animals that were forcibly killed before the expiration of these terms can be used as food for fur-bearing animals. Milk of dairy cows during and after the use of Inoxel is allowed to be used for food purposes without restrictions. Personal prevention measuresWhen working with Inoxel, you should follow the general rules of personal hygiene and safety, provided for when working with medicines. At the end of the work, wash your hands with warm water and soap.In case of accidental contact of the drug with the skin or mucous membranes of the eye, they should be washed with plenty of water. People with hypersensitivity to the components of the drug should avoid direct contact with Inoxel. In case of allergic reactions or accidental ingestion of the drug in the human body, you should immediately contact a medical institution (you should have the instructions for using the drug or the label). Empty vials from under the drug may not be used for household purposes, they are subject to disposal with household waste.Manufacturer:< / h3> < p>VETANCO S. A.; Chile 33 B 1603 CMA Vicinte Lopez, Buenos Aires, Argentina.

1. GENERAL INFORMATION 1.1. Ingaflor 10% solution (INGAFLOR 10% LIQUID) 1.2. Ingaflor 10% solution is an antibacterial drug in the form of a solution for oral administration, containing 100 mg / ml florfenicol as an active ingredient, as well as an auxiliary component - polyethylene glycol 400 to 1000 ml. 1.3. In appearance, the drug is a yellowish transparent viscous liquid, odorless, for the preparation of solutions with drinking water for animals. 1.4. The drug is produced packaged in high density polyethylene bottles with a capacity of 250 ml, 1L and 5L. 1.5. Store the medicinal product with precautions (list B), in a cool and dry place, protected from direct sunlight, at temperatures from + 5 ° C to + 25 ° C, avoiding freezing. Keep out of reach of children. 1.6. Shelf life of the veterinary medicinal product, in its original packaging: 2 years. Shelf life after opening the original packaging: 3 weeks. 2. PHARMACOLOGICAL PROPERTIES 2.1. Ingaflor 10% solution contains the active ingredient: florfenicol. The drug is used in veterinary medicine as an antibacterial agent. Florfenicol is a thiamphenicol derivative in which the hydroxyl group is replaced by a fluorine atom. Florfenicol has a bacteriostatic effect on sensitive microorganisms. In the protoplasm of a bacterial cell, it binds to the 70S ribosomal subunit, where it blocks the enzyme peptidyl transferase, which leads to inhibition of protein synthesis in sensitive bacteria at the ribosome level. Florfenicol is active against bacteria that produce acetyltransferase and are resistant to chloramphenicol. 3. ORDER OF APPLICATION OF THE PREPARATION 3.1. The drug is intended for the treatment of infections in poultry caused by microorganisms sensitive to florfenicol, such as Chlamydia, E. coli, Pasteurella, and Mycoplasma (for chlamydia, mycoplasmosis, CRD, necrotizing enteritis, colibacillosis, cholera), in pigs for the treatment of infections caused by Actinobacillus plepneumonia , Pasteurella species (P. multocida, P. haemolytica) and for the treatment of respiratory diseases caused by Haemophylus species. 3.2. The drug is used in birds and pigs. Ingaflor 10% solution is administered to birds orally with drinking water in a daily dose of 20 mg per 1 kg of body weight, which corresponds to: chickens under 4 weeks of age 150 ml of the drug per 100 liters of drinking water. For birds older than 4 weeks, 200 ml of the preparation per 100 l of water. Within 5 days. Ingaflor 10% solution is administered to pigs orally with drinking water in a daily dose of 10 mg florfenicol per 1 kg of body weight. (The average amount is equivalent to 100 ml "Ingaflor 10% solution" per 100 liters of drinking water). Within: 7 days. 4. PRECAUTIONS 4.1. When working with the drug, you should follow the general rules of personal hygiene and safety measures provided for when working with drugs. 5. PROCEDURE FOR SUBMISSION OF CLAIMS 5.1. In case of complications after using the drug, its use is stopped, and the consumer applies to the State Veterinary Institution in the territory in which he is located. Veterinary specialists of this institution conduct a study of compliance with all rules for the use of the drug in accordance with the instructions ... Upon confirmation of the detection of a negative effect of the drug on the animal's body, veterinary specialists take samples in the required amount for laboratory tests, write a sampling act and send it to the State Institution "Belarusian State Veterinary Center" for confirmation of compliance with regulatory documents. 6. MANUFACTURER 6.1. United Pharma, Hungary Instructions for the use of Ingaflor 10% solution prepared by the applicant Inga Pharm LLC, (Russia, 236016 Kaliningrad, Grazhdanskaya st., 28, building 11) < / p>

1. GENERAL INFORMATION 1.1. Ingaflor 10% oral powder (INGAFLOR 10% ORAL POWDER) 1.2. Ingaflor 10% oral powder is an antibacterial drug for oral administration, containing florfenicol 100 g as an active ingredient, and two excipients tixosil 1.0 g and dextrose monohydrate up to 1000 g. 1.3. In appearance, the drug is a white or almost white crystalline powder, odorless, for inclusion in animal feed. 1.4. The drug is produced packaged in multilayer polyethylene bags of 1 kg and 10 kg. 1.5. Store the drug with caution (list B), in a cool and dry place, protected from direct sunlight, at a temperature not lower than + 25 ° C. Keep out of reach of children. 1.6. Shelf life of the veterinary medicinal product, in its original packaging: 2 years. 2. PHARMACOLOGICAL PROPERTIES 2.1. Ingaflor 10% oral powder contains the active ingredient: florfenicol. The drug is used in veterinary medicine as an antibacterial agent. Effective in the treatment of infections caused by gram-positive and gram-negative bacteria. It is used to treat infections of pigs caused by microorganisms sensitive to the drug, such as Actinobacillus pleuropneumoniae, E. coli, Salmonella cholerae-suis, Pasteurella, Streptococcus suis, Mycoplasma, as well as some types of anaerobic microorganisms; and in fish for the treatment of furunculosis (peptic ulcer disease), as well as yersiniosis. 3. ORDER OF APPLICATION OF THE PREPARATION 3.1. Target animals: Pigs. Indications for use: pneumonia, enteritis and microorganisms sensitive to the drug. 3.2. Method of application and dosage: pigs 10 mg / kg body weight / day for 5 consecutive days with feed. For the treatment of enzootic pneumonia in pigs: Ingaflor 10% oral powder should be added to the feed add 10 mg of florfenicol per kg of body weight daily. The dose is 200-400 mg / kg of florfenicol in feed - the equivalent of 2 to 4 kg. Ingaflor 10% oral powder per ton of feed administered over 5 consecutive days. 4. PRECAUTIONS 4.1. When working with the drug, you should follow the general rules of personal hygiene and safety measures provided for when working with drugs. 5. PROCEDURE FOR SUBMISSION OF CLAIMS 5.1. In case of complications after using the drug, its use is stopped, and the consumer applies to the State Veterinary Institution in the territory in which he is located. Veterinary specialists of this institution conduct a study of compliance with all rules for the use of the drug in accordance with the instructions ... Upon confirmation of the detection of a negative effect of the drug on the animal's body, veterinary specialists take samples in the required amount for laboratory tests, write a sampling act and send it to the State Institution "Belarusian State Veterinary Center" for confirmation of compliance with regulatory documents. 6. MANUFACTURER 6.1. United Pharma, Hungary Instructions for the use of Ingaflor 10% oral powder were prepared by the applicant Inga Pharm LLC, (Russia, 236016 Kaliningrad, Grazhdanskaya st., 28, building 11)

GENERAL INFORMATION In appearance, the drug is a flowing yellow powder. The shelf life of the drug, subject to storage conditions in a sealed package, is 36 months from the date of production. The shelf life of liquid feed with the preparation is 12 hours. After opening the package, it is recommended to completely use up the product during therapy. It is forbidden to use after the expiration date. The medicinal product is produced in the form of a sterile powder packaged in 1 kg each in white polyethylene jars with a safety stopper, complete with a bottom lid and an insert, each packing unit is supplied with instructions for use. PHARMACOLOGICAL (BIOLOGICAL) PROPERTIES DOXIPHARM 50% - antibiotic, tetracycline group, ATC code Vet: QJ01AA02, intended for the treatment of broilers and pigs with diseases of bacterial and mycoplasma etiology. Tetracyclines are bacteriostatic antibiotics that inhibit protein synthesis necessary for the life of bacterial cells. Tetracyclines act by binding to the 30-S ribosome of bacteria through chelating bonds with the phosphate groups of messenger RNA. They also prevent the connection of transport RNA with messenger RNA ORDER OF APPLICATION DOXIPHARM 50% are used in pigs for the treatment of chronic respiratory diseases and other respiratory diseases, mainly caused by Pasteurella spp., Mycoplasma spp. ., Haemophilus gallinarum., Bordetella avium and Chlamydia psittaci. It is also used in pigs for the treatment of atrophic rhinitis and respiratory diseases, mainly caused by Actinobacillus spp. Bordetella bronchiseptica, Mycoplasma spp., Pasteurella multocida, Streptococcus suis. It is forbidden to use DOXIPHARMA 50% in animals with severe liver and kidney damage, with significant disorders in the development of cartilage tissue, with lesions of the nervous system, accompanied by convulsions; with hypersensitivity to doxycycline and tetracyclines. DOXIFARM 50% is used: for broilers - 4.0 g of the drug per 100 kg of animal weight (equivalent to 20 mg of doxycycline per 1 kg of animal weight), which corresponds to approximately 15-30 g of the drug per 100 liters of water for 3-5 days. pigs - 2.0 g of the drug per 100 kg of animal weight (equivalent to 10 mg of doxycycline per 1 kg of animal weight) for 3-5 days. It is recommended to divide the dose into two doses a day. PERSONAL PREVENTION MEASURES When working in DOXYFARM 50%, you should follow the general rules of personal hygiene and safety measures provided for when working with medicines ... When working with the drug, it is prohibited to drink, smoke and eat. After handling the medicine, wash your hands with soap and water. FULL NAME OF MANUFACTURER CHEMIFARMA S.p.A., Italy, Forlì, st. Via Don Eugenio Servadei, 16- 47100.

Viatoss adsorbent of mycotoxins in raw materials and feed for farm animals and poultry General information. Viatoss contains: ammonium salt, gelling agent (polyvinylpyrrolidone), colloidal aluminosilicates tri HSCAS with different charges and cation exchange capacity, micronized excipient. Release form - fine powder from brown to dark brown color. Biological properties. < p> Viatoss inactivates mycotoxins in contact with feed and in the intestines of animals and poultry. The process of inactivation of feed mycotoxins occurs in three different ways: silicate is aimed at the physical binding of polar mycotoxins - aflatoxin, zearalenone, T2 toxin, fumanisin; physical gelation of the gelling substance (3D lattice is formed) in the intestinal lumen; the process of chemical inactivation as a result of structural changes in the mycotoxin molecule, which is converted into net molecule (toxout). How to use it. Viatoss is added to the feed using the existing feed preparation technology. Recommended rates for the introduction of the Viatoss mycotoxin adsorbent ": for prophylaxis - from 500 g to 1.0 kg. per 1 ton of feed; with a low risk of contamination - from 1.0 kg to 1.5 kg per 1 ton of feed; with a high risk of contamination - up to 2.0 kg per 1 ton feed; Benefits of Viatoss The adsorbent does not cause side effects even at high rates of introduction. Products of farm animals and poultry after application of Viatoss can be used for food purposes without restrictions. Retains the activity of vitamins, minerals and other ingredients used for feeding in the feed itself and the small intestine. Manufacturer CHEMIFARMA SpA, Italy, Forli, Via Don Eugenio Servadei, 16-47100

General provisions In 1 ml. the drug contains 50 mg as an active ingredient. enrofloxacin. Excipients: propylene glycol-50 mg, potassium hydroxide-10 mg, benzyl alcohol-10 mg, methylparaben-1 mg, water for injection up to 1 ml. Bactyl 5 % injection is available in 100 ml vials. Pharmacological properties Enrofloxacin-quinolcarboxylic acid derivative belongs to fluoroquinols of the 3rd generation, has a wide spectrum of antibacterial action against gram-positive and gram-negative bacteria, in including Escherichia coli, Haemophilus spp., Pasteurella spp., Salmonella spp. Staphylococcus spp., Streptococcus spp., Clostridium perfmges, Bordetella bronchi- chiceptica, Campylobacter spp., Corinebacterium pyogenes, Pseudomonas spp. ... Cattle: slaughter of animals for meat is allowed no earlier than 14 days after the last use of the drug. The meat of animals that were forcedly killed before the expiration of the established period can be used to feed fur-bearing animals. How to use the drug Bactyl 5% injection is prescribed for medicinal purposes in cattle, pigs, dogs and cats for the treatment of bronchopneumonia, enzootic pneumonia, colibacillosis, salmonellosis, streptococcosis, septicemia, genitourinary and other diseases caused by microorganisms sensitive to fluoroquinolones, as well as mixed and secondary infections in viral diseases. Pigs are used for the treatment of enzymes. pneumonia, atopic rhinitis, mastitis-metritis-agalactia syndrome. The drug is used once a day in calves, dogs and cats subcutaneously, intramuscularly in pigs. For calves and pigs: 1 ml per 10 kg of animal weight (5 mg of enrofloxacin per 1 kg of animal weight) for 3-5 days. Dogs and cats: 1 ml per 10 kg of animal weight (5 mg of enrofloxacin per 1 kg of animal weight) for 5 days. At x ronic and severe diseases - up to 10 days. Contraindications Do not use Bactyl 5% for dogs under 1 year old, because of the possibility of damage to the articular cartilage during the period of rapid growth, especially in dogs large breeds. Use Bactil 5% with caution in very large breeds up to 18 months of age due to their longer growth period. Do not use in cats under 8 weeks of age. Bactyl 5% is not recommended for disease prevention. Cats: In case of overdose, damage to the retina, including blindness, is possible. In case of accidental overdose, there are no antidotes, and treatment should be symptomatic. When conducting a study of target groups of animals, daily administration of the drug at a dose of 15 mg / kg for 21 days led to a recoverable visual impairment in cats. With a single daily administration of the drug for 21 days at a dose of 30 mg / kg, an irreparable impairment of visual function was observed. With a single daily administration of the drug at a dose of 50 mg / kg for 21 days, blindness is possible. Dogs: Sometimes skin reactions may occur, especially when using the drug for hunting greyhounds. Do not exceed the recommended dose. Do not enter drug to the same site when repeated injections. Use of the drug must comply with local veterinary legislation. Fluoroquinolones should be used when the effectiveness of other antibiotics is in doubt and should remain stock antibiotics. < br> Fluoroquinolones should be used only after an antibiogram for sensitivity. Do not use lactating animals whose milk is used as food for humans. Do not use Bactyl 5% injection together with bacteriostatic antibiotics (levomycytin, macrolides and tetracyclines), theophylline and non-steroidal anti-inflammatory drugs. Manufacturer VETANCO S.A. company; Chile 33 B 1603 CMA Vicinte Lopez, Buenos Aires, Argentina.

General provisions "Antitox" - "Antitoxum". The drug is a sterile, transparent liquid with a specific smell of sulfur. 1.0 cm3 of the drug contains sodium thiosulfate pentahydrate 0, 2 g; sodium glutamate 0.022 g; chlorocresol 0.001 g; sodium bisulfite 0.0005 g; water for injection up to 1.0 cm3. The drug is produced packaged at 50.0; 100.0; 250.0 cm3 in glass vials. The drug is stored in the manufacturer's packaging according to the list in a dry, dark place at a temperature from + 5 ° C to + 25 ° C. Shelf life of the drug) years from the date of manufacture, subject to compliance rules for transportation and storage. Pharmacological properties The drug "Antitox" is intended for detoxification of the body by binding toxic products with the formation of non-toxic sulfites in case of poisoning with arsenic, mercury, lead and low-toxic rhodanic substances poisoning with hydrocyanic acid and its salts, iodine and bromine salts, ammonia utilization to urea. The resulting non-toxic compounds are excreted in the urine. The drug has a stabilizing effect on the membranes of hepatocytes, improves their energy supply, normalizes protein, carbohydrate and fat metabolism, increases the body's resistance to hypoxia. The drug helps to optimize the transport and use of oxygen in tissues, normalize the acid-base state of the blood, stimulate the transmission of excitation in the synapses of the central nervous system, increase the synthesis of protein and RNA in the liver tissue, preventing the development of hepatic coma in case of poisoning with hepatotropic poisons. Antitox "Improves the endocrine, immune and metabolic functions of the body, which play a major role in the prevention of multiple organ failure in critical conditions, which is an important condition for the treatment of this condition. How to use the drug The drug is used in as an antidote and hepatoprotector in case of poisoning with compounds of heavy metals, arsenic, cyanides, nitrates, nitrites, iodine and broma salts, as well as in mycotoxicosis and toxicosis of pregnant women. The drug is used in complex therapy In the treatment of metabolic disorders, liver dysfunction (hepatic coma), uremic syndrome, allergic dermatitis, eczema, acetonuria, acidosis, agalactia, anorexia, pododermatitis, neuritis, The drug is administered slowly, intravenously, intramuscularly, subcutaneously or intraperitoneally, once a day, until recovery in doses (per animal, ml): horses, cattle 40.0; pigs, sheep and goats 20 , 0-30.0; dogs 5.0-15.0; cats, rabbits, minks 3.0-5.0; guinea pigs, chinchillas, hamsters 1.5. If necessary, in severe cases of the disease) the dose of the drug should be doubled. The temperature of the drug at the time of administration should not be lower. There are no contraindications to the use of the drug. During pregnancy and lactation, the use of the drug does not wash away the negative effect on the condition of the animal and the fetus. As a result of individual intolerance, during the jet intravenous administration of dogs and cats are vomiting, Slaughter of animals for meat is allowed without a waiting period. Personal precautions When working, you should follow the rules of personal hygiene and safety measures provided for working with medicines ... Does not pose a Danger for the environment. Manufacturer ImmCont ImmCont GmbH), (Address: Angermunder Str16227 Eberswalde, Germany)

General information ANPROSOL AMINOBETA (ANPROSOL AMINOBETA is a feed additive for normalizing metabolism in all types of animals and poultry (regulator of liver function). It is a multicomponent mixture of water-soluble vitamins and amino acids, does not contain. As an active ingredient in 1 liter contains vitamin 110,000 mg, vitamin 24,000 mg, vitamin 64,000 mg, vitamin 1220 mg, vitamin 10 mg, pantothenic acid 22,000 mg, vitamin PP 45,000 mg, inositol ( vitamin 85 500 mg, chloride 200 000 mg and essential amino acids 8 530 mg in total. In appearance it is a transparent liquid from brown to brown, highly soluble in water. Biological properties < / strong> Vitamin 1- takes part in water, carbohydrate, protein and phosphorus metabolism.Participates in the transmission of nerve impulses and nervous excitement.Prevents oxidation of vitamins C and 6 participates in the synthesis of glycogen, fats, protein, nuc leic acids, stimulates the consumption of feed, creating conditions for the normal growth and development of farm animals and poultry. Vitamin 2- is part of 30 recovery processes, participates in the process of absorption and use of fats, the construction of hemoglobin molecules. Affects the correct metabolism of proteins and carbohydrates. Vitamin D-pantothenic acid (B3) - is an active part of many enzymes, is closely related to the metabolism of many B vitamins. Choline chloride is a carrier of mobile methyl groups. It is a constituent element of phospholipids. Choline is essential for the normal maturation of cartilage tissue and prevention of pecking, participates in fat metabolism of the liver, preventing fatty degeneration. Vitamin PP (B5) - in the body is converted into pantothenic acid and acquires its function. Stimulates the secretory function of the digestive glands, plays an important role in lipid metabolism, the metabolism of certain amino acids, participates in the Krebs cycle. Vitamin B6 - participates in the synthesis and breakdown of amino acids, fat, protein and energy metabolism, collagen synthesis. Inositol - is an integral part of lipoproteins, changes the concentration of calcium in the cytoplasm of the cell, activating calcium channels. Vitamin B12 - regulates the process of hematopoiesis, has a methionine-saving effect, is necessary for the normal activity of the mucous membrane of the gastrointestinal tract. Vitamin H - is part of the series enzymes, is involved in carbohydrate metabolism, the metabolism of cholesterol and nucleic acids, the development of immunity against infectious diseases. Amino acids are non-hydrolyzable proteids containing functional acidogroups - COOH and functional groups of primary amines - NH2 in their structure, participate in the formation of neurotransmitters, have antidepressant activity, participating comfort in the formation and accumulation of glycogen in muscles and liver, are part of proteins and contribute to muscle building. They stimulate the work of the pituitary gland, increase the production of growth hormone, take part in hematopoiesis, and above all in the production of hemoglobin. How to use ANPROSOL AMINOBETA is used to normalize work liver, metabolism and an increase in natural resistance in farm animals and poultry during the period of intensive growth, as well as an antistress agent during vaccination, restoration of intestinal microflora. Applied orally with water for drinking daily for 5-10 days at the rate of: poultry: 100-200 ml per 100 liters of drinking water per day; large animals (cattle, pigs, horses): 20-30 ml per head per day; small animals (sheep, goats, pigs, calves and foals): 5 ml per head per day. If necessary, the course can be extended up to 15 days. The working solution is prepared immediately before use, taking into account the daily consumption of liquid and the required concentration. Do not use cor new supplement ANPROSOL AMINOBETA in the drinking system together with oral vaccines and organic acids. Advantages ANPROSOL AMINOBETA contains vitamins and amino acids for which there is no period expectations, that is, products from farm animals and poultry can be used for food purposes without restrictions. The synergism of the action of vitamins and amino acids normalizes the functions of various enzyme systems of the body, which has a positive effect on metabolism and increases the natural resistance of the body, improves the average daily weight gain and safety of livestock. Manufacturer CHEMIFARMA SpA, Italy, Forli, Via Don Eugenio Servadei street, 16-47100

PHARMACOLOGICAL PROPERTIES AMOXIFARM is an antimicrobial drug, the only pharmacological active substance of which is amoxicillin, i.e. beta-lactam antibiotic. Amoxicillin trihydrate, which is a part of the drug, is a semisynthetic antibiotic of the penicillin series, has a wide spectrum of bactericidal action against gram-positive and gram-negative microorganisms, such as: Pasteurella multocida, Ornithobacterium rhinotracheale, Bordetella rhinotracheale, Bordetella rhinotracheale, Bordetella avium, Stapridium aphroxus, is an antibiotic of Clorysstapridium perfrigin a wide range of semisynthetic penicillins. It has a bactericidal effect caused by interference with mucopolysaccharides in the structure of the bacterial wall; this causes disruption of the cell wall and subsequent lysis of the bacteria. It is active against the main pathogenic bacteria, both gram-positive and gram-negative. In particular, it is used in the treatment of bacterial infections in broilers, turkeys and pigs, such as: respiratory infections (bronchitis, pneumonia, bronchopneumonia, pleurisy, pulmonary complications of viral infections); infections of the gastrointestinal tract (enteritis, cholangiohepatitis); urinary tract infections (nephritis, cystitis); genital infections; skin infections; joint infections. The antibiotic is excreted in active form, mainly through the urine. Has a quick therapeutic effect. Practically non-toxic, amoxicillin is well tolerated by animals. According to the degree of impact on the body, AMOXIPHARM refers to moderately hazardous substances (hazard class 3 according to GOST 12.1.007-76). INDICATIONS FOR USE AMOXIFARM is indicated for broilers, turkeys and pigs with infections supported by gram-positive and gram-negative bacteria susceptible to amoxicillin, in particular Pasteurella multocida, Ornithobacterium rhinotracheale, Bordetella avium, Clostridium perfringens, Staphylococcus aureus, Erysipelothrix rhusiopathiae in cases of colibacillosis gastrointestinal and urinary tract infections, skin infections, joint infections; in the treatment of clostridiosis caused by Clostridium perfringens. Dosage Broilers, turkeys and pigs: give orally a dose of 0.1-0.2 g / 10 kg of live weight per day (corresponds to 8-16 mg of amoxicillin trihydrate / kg of live weight / day), dissolved in drinking water for 3 5 days in a row. In particular, the approximate daily doses of AMOXIPHARMA are as follows: Broilers and turkeys: - during the first 4 weeks of life: 6-12 g / 100 liters of water consumed - over 4 weeks: 10-20 g / 100 water consumed per day Pigs: - up to 6 months of age: 10-20 g / 100 liters - over 6 months: 15-30 g / 100 liters It is recommended to give AMOXIFARM once a day together with drinking water CONTRAINDICATIONS Forbidden apply AMOXIFARM with solid feed! Simultaneous administration of other bacteriostatics such as tetracyclines, macrolides, sulfa drugs and quinolones is not allowed. A synergistic effect occurs when amoxicillin is administered concurrently with cloxacillin, polymyxins such as colistin and aminoglycosides such as streptomycin, neomycin, gentamycin and kanamycin. Rapid onset of cross-resistance with penicillins, especially ampicillin. The combination with clavulanic acid enhances the effect of the drug. SPECIAL INSTRUCTIONS Slaughter of animals for meat is not allowed earlier: broilers - 1 day, pigs - 1 day, turkeys - 2 days. Do not administer to a bird that lays eggs for human consumption. The meat of animals that were forcedly killed before the expiration of the established period can be used to feed fur animals.

< p>GENERAL INFORMATION < p>1.1. The product "ABSOLUTSID dikvat" is a clear liquid without mechanical impurities from weak to intensely yellow color with a characteristic smell. The product "ABSOLUTSID diquat" as active ingredients contains a complex of 2 quaternary ammonium compounds (H): alkyldimethylbenzylammonium chloride 4.9% and alkyldimethylethylbenzylammonium chloride 4.9%, as well as functional components, including buffer, stabilizing and anticorrosive additives. The pH of 1% of the working solution of the agent is 7.0±1.0. The product mixes well with water, has cleaning and deodorizing properties, and does not spoil the treated objects. Water solutions of the product have a slight specific smell, or the smell of the introduced fragrance. The shelf life of the product in the unopened packaging of the manufacturer is 5 years. The shelf life of working solutions is 35 days. The product retains its properties after freezing and thawing. The product is available in a polymer container with a capacity of 1 l to 30 l, which ensures the safety of the product during the entire shelf life, according to the current regulatory documentation. 1.2. The agent "ABSOLUCID diquat" has antimicrobial activity against Gram-negative and Gram-positive (including Mycobacterium tuberculosis) microorganisms, viruses (against all known viruses-human pathogens, including viruses of enteral and parenteral hepatitis (including hepatitis A, B and C), HIV, polio, adenoviruses, viruses of "SARS", "avian" influenza H5N1, "swine" influenza, human influenza, herpes, etc.), fungi of the genus Candida, Trichophyton and mold fungi, pathogens of nosocomial infections; the agent has ovocidal properties against pathogens of parasitic diseases (cysts and oocysts of protozoa, eggs and larvae of helminths, pinworms). 1.3. In the parameters of acute toxicity (LD50, when introduced into the stomach) means "ABSOLUTE Diquat" refers to the 4th class of low-dangerous substances in accordance with GOST 12.1.007-76 and 5 class practically non-toxic substances, when injected into the peritoneum according to the classification of K. K. Sidorova, as well as to low-hazard substances largest DL50 when applied to the skin (grade 4 little dangerous substances in accordance with GOST 12.1.007-76). When inhaled in the form of vapors according to the degree of volatility (C20), the agent is not very dangerous; in the form of an aerosol, the agent has a general toxic effect corresponding to the threshold of acute single action. The concentrate of the product has a pronounced irritating effect on contact with the skin and conjunctiva of the eye. The product has no sensitizing activity. Working solutions with repeated applications can cause dryness and peeling of the skin (in concentrations above 2%), and in the form of an aerosol have an irritating effect on the mucous membranes of the eyes and respiratory tract. Working solutions do not have a general toxic effect in contact with the skin and the effect of sensitization. MPC HOUR in the air of the working area of 1 mg / m3, aerosol. 1.4. Means "ABSOLUTE Diquat" is designed to: - disinfection and washing of surfaces in rooms, hard and soft furniture, floor coverings and upholstery fabrics, furnishings, surfaces of devices, appliances, sanitary equipment, linen, dishes (including disposable and laboratory), items for washing dishes, rubber and polypropylene mats, cleaning equipment and materials, toys, sports equipment, patient care items, personal hygiene items in medical institutions and medical institutions (including clinical, diagnostic and bacteriological, virological, PCR and other laboratories, neonatology departments, maternity hospitals, wards of newborns, etc.), in children's and penitentiary institutions, in infectious foci during current, final and preventive disinfection; - disinfection of couvezes and devices for them, components of anesthesia, inhalation equipment, anesthetic equipment; - for disinfection of medical waste-single-use medical products, dressings, single-use underwear, etc. before their disposal in the medical facility, as well as food and other (liquid waste, blood, flushing water (including endoscopic flushing water), patient discharge (sputum, urine, feces, vomit, etc.), dishes from under the patient's discharge) waste;-disinfection of dental impressions made of alginate, silicone materials, polyester resin, dental prosthetic blanks made of metals, ceramics, plastics and other materials, suction systems of dental installations, salivators and spittoons; - disinfection of medical devices (including surgical and dental instruments, including rotating, rigid and flexible endoscopes, instruments for endoscopes) by manual means; - disinfection, combined with pre-sterilization cleaning, of medical devices (including surgical and dental instruments, including rotating, instruments for endoscopes) by manual and mechanized methods (in ultrasound installations of any type) ; - disinfection combined with pre-sterilization or final (before high-level disinfection (TLD)) cleaning of flexible and rigid endoscopes by manual and mechanized methods (in specialized installations, for example, "KRONT-UDE"); - pre-sterilization cleaning, not combined with disinfection, of medical products (including endoscope instruments, surgical and dental instruments, including rotating ones, as well as dental materials) by manual and mechanized methods (in ultrasound installations of any type) ; - pre-sterilization cleaning, not combined with disinfection, of rigid and flexible endoscopes by manual and mechanized methods (in specialized installations, for example, "KRONT-UDE"); - final cleaning of endoscopes before the TLD by manual and mechanized methods (in specialized installations, for example, "KRONT-UDE"); - pre-cleaning of endoscopes; - disinfection of shoes made of rubber, plastic and other polymer materials in order to prevent fungal infections (dermatophytosis); - disinfection of sanitary transport and transport for the transport of food products; - disinfection, including irrigation, rolling stock and infrastructure of the automobile and urban electric passenger transport; - disinfection, including irrigation, surfaces, and objects in ships sea and river fleet, engaged in passenger and freight transport, ships, boats, mother ships, etc. of the Navy, as well as port infrastructure; on fishing boats, trawlers, floating and stationary processing plants, etc.; - carrying out General cleaning in health care, child care, school and other educational and health institutions and organizations, municipal facilities, penal and other institutions and organizations; - combat mold; - disinfection of air sputtering method at various sites, preventive disinfection of ventilation and air conditioning (room air conditioners, split-system, multi-zone split systems, rooftop air conditioners, ventilation filters, ducts, etc.); - disinfection and washing of premises and equipment (including equipment that has contact with food products) at public catering enterprises, food trade, consumer markets, municipal facilities, hotels, dormitories, swimming pools, water parks, baths, saunas, places of mass gathering of people; - disinfection of premises, equipment, tools, workwear, air of hairdressers, massage and beauty salons, beauty salons, laundries, clubs, sanitary facilities and other public service facilities; - disinfection, cleaning, washing and deodorizing of garbage collection equipment, garbage trucks, garbage cans and garbage collectors, garbage chutes; - decontamination of the contents of storage tanks of autonomous toilets that do not have a drain to the sewer, as well as surfaces in the cabins of autonomous toilets and bio-toilets; - use in dezkovriki; - disinfection of soil, household items, toys, premises, laboratory utensils and laboratory equipment contaminated with pathogens of parasitic diseases (cysts and oocysts of protozoa, eggs and larvae of helminths, pinworms); - for disinfection of the surface of the shell of raw and boiled eggs before eating; - for disinfection of eggs in poultry farms before sending to the retail network; - for disinfection of poultry eggs before laying in incubators; - for disinfection of eggs in virological laboratories before performing work on obtaining chicken embryos. < p> PREPARATION OF WORKING SOLUTIONS.Solutions of "ABSOLUTE Diquat" serves in the capacity of any material by mixing tool with tap water. In the preparation of working solutions should be guided by the calculations shown in table 1. ATTENTION! Solutions of the product for various manual processing of any objects can be used repeatedly during the shelf life (35 days), if their appearance has not changed. When the first signs of a change in appearance (color change, turbidity of the solution, precipitation, etc.) appear, the solution must be replaced before the expiration of the specified period. Solutions of the product for disinfection combined with pre-sterilization cleaning, and for pre-sterilization cleaning of medical products in a mechanized way in ultrasonic or other specialized installations can be used repeatedly during a working shift or a working day, if their appearance has not changed. When the first signs of a change in appearance (color change, turbidity of the solution, precipitation, etc.) appear, the solution must be replaced before the expiration of the specified period.PRECAUTIONSWhen preparing working solutions, it is necessary to avoid contact with the skin and eyes.

The feed additive GFO LIVESTOCK is used in the diet of poultry as a complex drug that: - strengthens the immune system, increases its resistance to diseases, unfavorable factors (stress, temperature changes, etc.); - stimulates the processes of hematopoiesis and mineral metabolism; activates and normalizes digestion processes; - promotes better digestion and assimilation of feed, increases appetite; - has a direct antiviral effect; - provides an increase in the productivity and safety of poultry from gastrointestinal and respiratory diseases: - poultry growth accelerates and productivity increases. Feeding poultry additionally gives an increase in muscle mass, which increases by 10-25%, mortality decreases, feed costs are reduced by 10-20% increase in egg production, improve the quality of meat, reduce the cost of honey. preparations. Application rates: added to food and drink 0.1 -0.5 ml per 1 kg of weight. Proportions, application: 5 - 1 0 l. product, per 1 ton of feed or ton of water Ingredients: 16 natural water-soluble amino acids, incl. histidine, glycine, methionine, etc., natural vitamins: A, B1 -B12, E, C, D, P; humic acid and fulvic acid; nitrogen (N), phosphorus (P), potassium (K) and trace elements: Mn, Cu, B, Zn, I, Mg, etc. We are interested in long-term cooperation with farms, agricultural companies, and also companies selling microfertilizers, housing and communal services, feed additives for animals, poultry, fish.

Extruded feed for carp from 46 rubles / kg: Granule size, mm: 2, 3, 6, 8, 10 Protein,%: 35 Total fat ,%: 6 Carbohydrates,%: 30.8 Ash,%: 8.36 Fiber,%: 4.16 Starch,%: 13.18 Total energy, kcal: 4791.9 - Metabolic energy, kcal: 3583.06.

Extruded feed for sturgeon from 57 rubles / kg: Granule size, mm: 2, 3, 6, 8, 10 Total protein,%: 45 Total fat,%: 15 Carbohydrates,%: 26 Ash,%: 11.6 Fiber,%: 1.8 Starch,%: 2.99 Total energy Kcal: 5262 Metabolic energy Kcal: 4131.

Extruded compound feed for trout from 57 rubles / kg: Granule size, mm: 2, 3, 6, 8, 10 Total protein,%: 45 Total fat,%: 15 Carbohydrates,%: 26 Ash,%: 11.6 Fiber,%: 1.8 Starch,%: 7.8 Total energy Kcal: 5262 Exchange energy Kcal: 4131

< p>FEATURES AND BENEFITS: The combination of the active components-enrofloxacin and colistin sulfate-having a synergistic effect, provides a wide range of antibacterial and mycoplasma effects.The combination of enrofloxacin and colistin sulfate prevents the rapid development of resistance of microorganisms to fluoroquinolones.Ease of dosage and application.Short course of treatment — 5 days!Description: Arrestin — a broad-spectrum drug for the treatment of diseases of antibacterial and mycoplasma etiology.Enrostin is prescribed for therapeutic purposes to young cattle and small cattle, pigs and poultry for respiratory and gastrointestinal diseases, colibacteriosis, salmonellosis, streptococcosis, necrotic enteritis, hemophilosis, mycoplasmosis, mixed and secondary infections in viral diseases and other diseases whose pathogens are sensitive to enrofloxacin and colistin.Description: Arrestin — a broad-spectrum drug for the treatment of diseases of antibacterial and mycoplasma etiology.Enrostin is prescribed for therapeutic purposes to young cattle and small cattle, pigs and poultry for respiratory and gastrointestinal diseases, colibacteriosis, salmonellosis, streptococcosis, necrotic enteritis, hemophilosis, mycoplasmosis, mixed and secondary infections in viral diseases and other diseases whose pathogens are sensitive to enrofloxacin and colistin.General information: 1.Trade name of the medicinal product: Arrestin (Enrostin).International nonproprietary name: enrofloxacin, colistin. 2. Dosage form: solution for oral administration.Enrostin as active ingredients in 1 ml contains: enrofloxacin-100 mg and colistin sulfate-106 IU, as well as auxiliary substances: benzyl alcohol, sodium metabisulfite, lactic acid, synthanol and purified water.3. In appearance, the drug is a liquid from light yellow to yellow in color; during storage, a slight turbidity is allowed, which disappears after shaking.The shelf life of Enrostine under the conditions of storage in the closed packaging of the manufacturer is 2 years from the date of production, after opening the bottle-no more than 28 days. < p>The use of Enrostine after the expiration date is prohibited.4. Enrostin is produced packaged in 5 and 10 ml glass and polymer dropper bottles, complete with screw-on lids and dropper stoppers, and 100 ml in polymer bottles, complete with screw-on lids. Vials of 5, 10 and 100 ml are packed individually, vials of 5 and 10 ml are also packed in 10 vials in packs of cardboard, complete with instructions for use. Bottles of 1 liter of polymer materials are sealed with lids and provided with instructions for use. 5. Store the drug in the closed packaging of the manufacturer, in a place protected from direct sunlight, separate from food and feed, at a temperature of 5 °C to 25 °C.6. Arrestin should be stored in places inaccessible to children.7. Unused medicinal product is disposed of in accordance with the requirements of the legislation.8. Conditions of release: without a prescription from a veterinarian. < p>Pharm. Sv-va: 9. Arrestin refers to a combination of antibacterial drugs. 10. The combination of enrofloxacin and colistin sulfate, which are part of the drug, provides a wide range of its antimicrobial activity. Enrofloxacin belongs to the fluoroquinolone group of compounds, the mechanism of action of which is based on inhibition of the activity of the gyrase enzyme affecting replication of DNA spiral in nucleus of bacterial cells, leading to suppression of growth and development of gram-positive and gram-negative bacteria, including Escherichia coli, Haemophilus spp., Pasteurella spp., Salmonella spp., Staphylococcus spp., Streptococcus spp., Clostridium perfringens, Bordetella spp., Campylobacter spp. Corynebacterium pyogenes, Pseudomonas aeruginosa and Mycoplasma spp.Colistin Sulfate – the compound of a group of polypeptide antibiotics, disrupting the permeability of the bacterial cell wall by combining with lipoproteins, causes changes in intracellular metabolism and the death of Gram-negative bacteria, including Escherichia coli, Pseudomonas aeruginosa, Klebsiella spp., Salmonella spp., Proteus spp.After oral administration of the drug, enrofloxacin is well and quickly absorbed in the gastrointestinal tract and penetrates into most organs and tissues; excreted unchanged and partially as metabolites, mainly with urine and in small amounts in feces; colistin sulfate is practically not absorbed in the gastrointestinal tract, does not accumulate in the organs and tissues of the body are excreted mainly unchanged in the faeces. According to the degree of exposure to the body, Enrostine belongs to moderately dangerous substances (hazard class 3 according to GOST 12.1.007-76), in recommended doses it is well tolerated by animals, does not have embryotoxic and teratogenic properties.Application procedure: 12. Contraindication to use is the hypersensitivity of the animal to the components of the drug. It is forbidden to use Enrostin to laying hens and repair young animals less than 2 weeks before the start of egg laying, due to the accumulation of enrofloxacin in the eggs. It is not allowed to use Enrostin in adult ruminants with developed cicatricial digestion, piglets weighing less than < p>20 kg, animals with severe disorders of the development of cartilage tissue, severe kidney and/or liver diseases, with lesions of the nervous system accompanied by convulsions, pregnant and lactating sows.13. Enrostin is administered to animals orally once a day for 3 to 5 days, in the following doses: - calves, lambs, pigs-0.3 ml/kg of animal weight, drinking with water for drinking in a 1:1 dilution; in the severe form of the disease, the daily dose of the drug is increased to 0.5 ml/kg of animal weight; < p>- broilers, breeding poultry, repair young chickens, parent broiler herd and meat turkeys – 0.5 ml/l of water for drinking.In salmonellosis, mixed infections, as well as in chronic forms of avian diseases, the course of treatment is extended to 7 days.During the treatment period, the bird should only receive water containing the drug. The therapeutic solution is prepared daily in a volume calculated for the consumption of poultry during the day.14. With an overdose of the drug, the animal may experience a decrease in appetite, depression, vomiting, diarrhea. 15. Features of the action at the first use of the drug and at its cancellation were not revealed. 16. It is not allowed to use Enrostin to pregnant and lactating sows, as well as laying hens and repair young animals less than 2 weeks before the start of egg laying.17. You should avoid skipping the next dose of the drug, as this can lead to a decrease in effectiveness. In case of missing one dose, the use of the drug is resumed at the same dose according to the same scheme.18. When applying Annastina in accordance with this instruction side effects and complications are usually not observed. With increased individual sensitivity to the components of the drug and the development of allergic reactions, the use of Enrostine is discontinued and desensitizing therapy is performed.19. Enrostin should not be used simultaneously with levomycetin, macrolides, tetracyclines, theophylline, polyester ionophores, nonsteroidal anti-inflammatory drugs, drugs containing magnesium, aluminum and calcium cations, which, binding to enrofloxacin, prevent its adsorption.20. Slaughter of birds for meat is allowed no earlier than 11 days; calves, lambs and pigs-no earlier than 14 days after the last use of the drug. The meat of animals that were forcibly killed before the expiration of these terms can be used as food for fur-bearing animals.Preventive measures: 21. When working with Enrostine, you should follow the general rules of personal hygiene and safety, provided for when working with medicines. 22. It is forbidden to smoke, drink or eat while working. At the end of working with the drug, you should thoroughly wash your face and hands with soap. Empty packaging from under the drug is forbidden to use for household purposes, it is subject to disposal with household waste. People with hypersensitivity to the components of the drug should avoid direct contact with the drug Enrostin.23. If the drug gets on the skin or mucous membranes, it is necessary to immediately wash them with plenty of water. In case of allergic reactions or accidental ingestion of the drug in the human body, you should immediately contact a medical institution (you should have the instructions for use or the label). Name and address of the production site of the manufacturer of the medicinal product for veterinary use: LLC NPO Api-San, Moscow region, Balashikha district, Poltevskoe highway, possession 4.Name, address of the organization authorized by the holder or owner of the registration certificate of the medicinal product to accept claims from the consumer: LLC NPO Api-San, Moscow region, Balashikha district, Poltevskoe highway, possession 4.

LLC "Karavan fodder yeast plant" produces and sells fodder yeast, dry, inactive, made on after alcohol grain stillage. Caravan yeast will harmoniously complement compound feed for cattle, their use increases milk yield and productivity growth. Quality our products have been appreciated by many livestock farms. The resulting yeast is rich in vitamins, essential amino acids, proteins and trace elements. Can be partially replaced as part of feed fish, meat, blood meal, as well as soybean meal and cake - what reduces your cost per unit. - possess the ability to absorb mycotoxins; - their use excludes danger of disease of animals and birds with candidiasis; - provide the body animals with amino acids, vitamins groups B, D, C and do not contain chlorides; - their use is significant enhances immunity and physiological characteristics of birds and animals. Terms of delivery: EXW - seller's warehouse. (Lyubotin, Kharkiv region) Packaging - bags 25 kg , or big bags, term storage - 6 months.