Select A LocationAIVLOSIN® 17%
(Tylvalosin Type A Medicated Article)
VFD Forms
Product Description
- Aivlosin 17% contains the macrolide antibiotic Tylvalosin and is used for the manufacture of Type B and Type C medicated feeds
- Tylvalosin medicated feed is used for the control of ileitis in swine
- Not to be fed undiluted
- Free-flowing granules
- 50-lb bags
Key Features
- Available for pigs as an in-feed medication for ileitis control
- Broad spectrum, potent macrolide not used in human health
- Reliable dosing, consistent mixing
- No withdrawal period (0 days)
- Wide safety margin
Label Indications and Dosage
Caution: Federal law restricts medicated article containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.
For Swine: Control of porcine proliferative enteropathy (PPE) associated with Lawsonia intracellularis infection in groups of swine in buildings experiencing an outbreak of PPE.
Feeding Directions: Feed Type C medicated article containing 38.6 grams tylvalosin/ton as the sole ration for 14 consecutive days.
Caution: To assure both food safety and responsible use in swine, concurrent use of tylvalosin Type A medicated article in medicated article and tylvalosin or another macrolide in medicated drinking water or by any other route of administration should be avoided. Not for use in swine intended for breeding. The effects of tylvalosin on swine reproductive performance, pregnancy, and lactation have not been determined. VFDs for tylvalosin shall not be refilled.
Mixing Directions:
Preparation of Type B medicated feed containing 3,856 grams per ton (4,250 ppm) tylvalosin: Prepare tylvalosin Type B medicated article in mash form only. To manufacture one ton of Type B medicated article containing 3,856 g/ton (4,250 ppm) tylvalosin, mix 50 pounds of Aivlosin ® 17% Type A Medicated Article with 1950 pounds of non-medicated feed.
Preparation of Type C medicated feed containing 38.6 grams per ton (42.5 ppm) tylvalosin: To manufacture one ton of Type C medicated feed containing 38.6 g/ton (42.5 ppm) tylvalosin, mix 0.5 pound of Aivlosin® 17% Type A Medicated Article with 1999.5 pounds of non-medicated feed. To aid in the even distribution of drug in the finished feed, add the full amount of Aivlosin® 17% Type A Medicated Article into a small portion of the feed and mix. Blend this mixture into the remainder of the feed and mix thoroughly.
Pelleted Type C medicated feeds must bear an expiration date of 30 days after the date of manufacture.
Crumbled Type C medicated feeds must bear an expiration date of 7 days after the date of manufacture.
Antibacterial Warnings: Use of antibacterial drugs in the absence of a susceptible bacterial infection is unlikely to provide benefit to treated animals and may increase the development of drug-resistant bacteria.
User Safety Warnings: Not for use in humans. Keep out of reach of children. May cause skin irritation. Tylvalosin has been shown to cause hypersensitivity reactions in laboratory animals. People with known hypersensitivity to tylvalosin should avoid contact with this product. In case of accidental ingestion or inhalation, seek medical attention. When handling Aivlosin 17% Type A Medicated Article and preparing medicated feeds, avoid direct contact with the eyes and skin. Wear a dust mask, coveralls and impervious gloves when mixing and handling this product. Eye protection is recommended. In case of accidental eye exposure, wash eyes immediately with water and seek medical attention. If wearing contact lenses, immediately rinse the eyes first, then remove contact lenses and continue to rinse the eyes thoroughly and seek medical attention. In case of accidental skin exposure, wash contaminated skin thoroughly.
The Safety Data Sheet contains more detailed occupational safety information.
Withdrawal Period
- No withdrawal period is required before slaughter for human consumption.
- Different withdrawal times may be required for certain export markets.
Packaging
- 50 lb (22.7 kg) bags
Formulation
- Free-flowing granules.
- Formulated for optimal dispersion, segregation, and stability in feed.
FDA Status
- Type A Medicated Article for use in the manufacture of Type B or Type C medicated article for swine.
- Category I drug; does not require a feed mill license.
- Veterinary feed directive required:Federal law restricts medicated article containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.
- Approved by FDA under NADA # 141-460
Swine
Caution: Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.
For Swine: Control of porcine proliferative enteropathy (PPE) associated with Lawsonia intracellularis infection in groups of swine in buildings experiencing an outbreak of PPE.
Feeding Directions: Feed Type C medicated feed containing 38.6 grams tylvalosin/ton as the sole ration for 14 consecutive days.
Caution: To assure both food safety and responsible use in swine, concurrent use of tylvalosin Type A medicated article in medicated feed and tylvalosin or another macrolide in medicated drinking water or by any other route of administration should be avoided. Not for use in swine intended for breeding. The effects of tylvalosin on swine reproductive performance, pregnancy, and lactation have not been determined. VFDs for tylvalosin shall not be refilled.
Mixing Directions:
Preparation of Type B medicated feed containing 3,856 grams per ton (4,250 ppm) tylvalosin: Prepare tylvalosin Type B medicated feed in mash form only. To manufacture one ton of Type B medicated feed containing 3,856 g/ton (4,250 ppm) tylvalosin, mix 50 pounds of Aivlosin ® 17% Type A Medicated Article with 1950 pounds of non-medicated feed.
Preparation of Type C medicated feed containing 38.6 grams per ton (42.5 ppm) tylvalosin: To manufacture one ton of Type C medicated feed containing 38.6 g/ton (42.5 ppm) tylvalosin, mix 0.5 pound of Aivlosin® 17% Type A Medicated Article with 1999.5 pounds of non-medicated feed. To aid in the even distribution of drug in the finished feed, add the full amount of Aivlosin® 17% Type A Medicated Article into a small portion of the feed and mix. Blend this mixture into the remainder of the feed and mix thoroughly.
Pelleted Type C medicated feeds must bear an expiration date of 30 days after the date of manufacture.
Crumbled Type C medicated feeds must bear an expiration date of 7 days after the date of manufacture.
Antibacterial Warnings: Use of antibacterial drugs in the absence of a susceptible bacterial infection is unlikely to provide benefit to treated animals and may increase the development of drug-resistant bacteria.
User Safety Warnings: Not for use in humans. Keep out of reach of children. May cause skin irritation. Tylvalosin has been shown to cause hypersensitivity reactions in laboratory animals. People with known hypersensitivity to tylvalosin should avoid contact with this product. In case of accidental ingestion or inhalation, seek medical attention. When handling Aivlosin 17% Type A Medicated Article and preparing medicated feeds, avoid direct contact with the eyes and skin. Wear a dust mask, coveralls and impervious gloves when mixing and handling this product. Eye protection is recommended. In case of accidental eye exposure, wash eyes immediately with water and seek medical attention. If wearing contact lenses, immediately rinse the eyes first, then remove contact lenses and continue to rinse the eyes thoroughly and seek medical attention. In case of accidental skin exposure, wash contaminated skin thoroughly.
The Safety Data Sheet contains more detailed occupational safety information.
Available in the USA
The labeling contains complete use information, including any cautions and warnings. Always read, understand and follow the labeling and use directions. See the reverse side for use directions and additional information.