{name} in bulk on Qoovee

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 LIFE" is used in the diet of animals as a complex preparation which: - 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 the appetite of animals; - has a direct antiviral effect; - provides an increase in the productivity and safety of animals from gastrointestinal and respiratory diseases: - the growth accelerates and the productivity of animals increases. Animal feeding additionally gives an increase in muscle mass, which increases by 15-30%, mortality decreases, feed costs are reduced 10-20 % (the animal reaches the required weight gain 2-3 months earlier than with normal feeding), the quality of meat improves, the cost of honey preparations is significantly reduced. Stimulates lactation in cows, an increase in milk yield by 15-20% and an increase in fat content milk . Application rates: added to feed and drink 0.3 -0.5ml per 1 kg of weight. (10-20l per 1 ton. Feed or 1 ton. Water) Produced in the form of a brown solution with a specific, not pungent odor. Composition: 16 natural water-soluble amino acids: histidine, glycine, methionine, etc., natural vitamins: A, B1 -B12, E, C, D, P; humic and fulvic acids; nitrogen (N), phosphorus (P), potassium (K) and trace elements: Mn, Cu, B, Zn, I, Mg, etc. Shelf life 1 year. Storage temperature +5 to + 25C We are interested in long-term cooperation with farms, agricultural firms, as well as companies selling microfertilizers, housing and communal services, feed additives for animals, birds, fish.

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.

Dark brown ammunition set. The seat allows the rider to feel comfortable and safe. The whole set is made in the national style. Material: genuine leather. When tailoring a saddle to order, various finishing options are possible.