Beef

Full Value Beef™

Full Value Beef™ is not a one-size-fits-all solution, it’s a customized approach based entirely on the specific needs of your operation. Whether we’re helping you uncover hidden profit opportunities using our data and analytic capabilities or expanding the tools and services that help you maximize return on our innovative products, it’s all about making sure you’re getting the full value of everything we have to offer. Learn more about how Full Value Beef applies to you as a veterinarian, nutritionist, feedyard, calf ranch or stocker, or stocker operator.

Important Safety Information hjs

For Micotil®:

Micotil is indicated for the treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida and Histophilus somni, and for the control of respiratory disease in cattle at high risk of developing BRD associated with Mannheimia haemolytica.

Before using this product, it is important to read the entire product insert, including the boxed human warning.

Caution: Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian.

• Not for human use. Injection of this drug in humans has been associated with fatalities. Keep out of reach of children. Do not use in automatically powered syringes. Exercise extreme caution to avoid accidental self-injection. In case of human injection, consult a physician immediately, and apply ice or cold pack to injection site while avoiding direct contact with the skin. Avoid contact with eyes.
• Always use proper drug handling procedures to avoid accidental self-injection. Consult your veterinarian on the safe handling and use of all injectable products prior to administration.
• For use in cattle or sheep only. Inject subcutaneously. Injection of this antibiotic has been shown to be fatal in swine and non-human primates, and may be fatal in horses and goats.
• Do not use in female dairy cattle 20 months of age or older. Use in lactating dairy cattle or sheep may cause milk residues.
• The following adverse reactions have been reported: in cattle: injection site swelling, and inflammation, lameness, collapse, anaphylaxis/anaphylactoid reactions, decreased food, and water consumption, and death.
• Micotil has a pre-slaughter withdrawal time of 42 days.

For Pulmotil®:

CAUTION: Federal law restricts medicated feed containing this veterinary feed directive (VFD) drug to use by or on the order of a licensed veterinarian.

• Cattle intended for human consumption must not be slaughtered within 28 days of the last treatment.
• To assure both food safety, and responsible use, treatment must be initiated within the first 45 days of the production period. The treatment should not occur concurrent with or following administration of an injectable macrolide, or within 3 days following administration of a non-macrolide injectable BRD therapy.
• VFD expiration date must not exceed 45 days from the time of issuance. VFDs shall not be refilled.
• Use only in cattle fed in confinement for slaughter.
• Cattle with severe clinical illness should be evaluated for individual treatment with an alternative non-macrolide therapy.
• Do not use in female dairy cattle 20 months of age or older or in veal calves.
• Safety has not been established for cattle intended for breeding.
• Do not allow horses or other equines access to feeds containing tilmicosin.
• Avoid inhalation, oral exposure, and direct contact with skin or eyes. Keep out of reach of children.

For Rumensin®:

• Consumption by unapproved species or feeding undiluted may be toxic or fatal. Do not feed to veal calves.

For Tylan® Injection:

• Injection of tylosin in equines has been fatal. Discontinue use in cattle 21 days before slaughter.

For Tylan®:

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 all products:

• The labels contain complete use information, including cautions and warnings. Always read, understand, and follow the labels and use directions.

Dosage/Use Levels

Rumensin®: Cattle fed in confinement for slaughter

For improved feed efficiency: Feed 5 to 40 g/ton of monensin (90% DM basis) continuously in a complete feed to provide 50 to 480 mg/hd/d.

For the prevention and control of coccidiosis due to Eimeria bovis and Eimeria zuernii: Feed 10 to 40 g/ton of monensin (90% DM basis) continuously to provide 0.14 to 0.42 mg/lb of body weight/d, depending upon severity of challenge, up to a maximum of 480 mg/hd/d.

Rumensin®: Growing cattle on pasture or in drylot (stockers, feeders, and dairy and beef replacement heifers)

For increased rate of weight gain: Feed 50 to 200 mg/hd/d of monensin in at least 1.0 lb of Type C medicated feed. Or, after the 5th day, feed 400 mg/hd/d every other day in at least 2.0 lbs of Type C medicated feed. The Type C medicated feed must contain 15 to 400 g/ton of monensin (90% DM basis).

For the prevention and control of coccidiosis due to Eimeria bovis and Eimeria zuernii: Feed at a rate to provide 0.14 to 0.42 mg/lb of body weight/d, depending upon severity of challenge, up to a maximum of 200 mg/hd/d. The Type C medicated feed must contain 15 to 400 g/ton (90% DM basis).

Free-choice supplements: Approved supplements must provide not less than 50 nor more than 200 mg/hd/d of monesin.

Rumensin: Mature reproducing beef cows

For improved feed efficiency when receiving supplemental feed: Feed continuously at a rate of 50 to 200 mg/hd/d. Cows on pasture or in drylot must receive a minimum of 1.0 lb of Type C medicated feed/hd/d. Do not self-feed.

For the prevention and control of coccidiosis due to Eimeria bovis and Eimeria zuernii: Feed at a rate of 0.14 to 0.42 mg/lb of body weight/d, depending upon severity of challenge, up to a maximum of 200 mg/hd/d.

Rumensin: Calves (excluding veal calves)

For the prevention and control of coccidiosis due to Eimeria bovis and Eimeria zuernii: Feed at a rate of 0.14 to 1.0 mg/lb of body weight/d, depending upon severity of challenge, up to a maximum of 200 mg/hd/d. The Type C medicated feed must contain 10 to 200 g/ton (90% DM basis).

Tylan®

For the reduction of incidence of liver abscesses associated with Fusobacterium necrophorum and Arcanobacterium pyogenes: Feed continuously as the sole ration at 8 to 10 g/ton of tylosin (90% DM basis) to provide 60 to 90 mg/hd/d.

Optaflexx®: Complete feed

For increased rate of weight gain, and improved feed efficiency: Feed 8.2 to 24.6 g/ton of ractopamine hydrochloride (90% DM basis) continuously in a complete feed to provide 70 to 430 mg/hd/d for the last 28 to 42 days on feed.

For increased rate of weight gain, improved feed efficiency, and increased carcass leanness: Feed 9.8 to 24.6 g/ton of ractopamine hydrochloride (90% DM basis) continuously in a complete feed to provide 90 to 430 mg/hd/d for the last 28 to 42 days on feed.

Optaflexx®: Top dress

For increased rate of weight gain, and improved feed efficiency: Feed 70 to 400 mg/hd/d of ractopamine hydrochloride (90% DM basis) continuously in a minimum of 1.0 lb/hd/d top dress Type C medicated feed (maximum 800 g/ton ractopamine hydrochloride) during the last 28 to 42 days on feed.

Pulmotil®

For the control of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, and Histophilus somni in groups of beef, and non-lactating dairy cattle, where active BRD has been diagnosed in at least 10% of the animals in the group: Feed continuously for a single, 14-day period at 568 to 757 g/ton of tilmicosin (100% DM basis) in a Type C medicated feed as the sole ration to provide 12.5 mg/kg of body weight/day.

Implants

Administer one dose in the ear subcutaneously according to label directions.

Tylan® Injection

For use in the treatment of bovine respiratory complex (shipping fever, pneumonia) usually associated with Pasteurella multocida and Arcanobacterium pyogenes; foot rot (necrotic pododermatitis) and calf diphtheria caused by Fusobacterium necrophorum and metritis caused by Arcanobacterium pyogenes: Inject intramuscularly 8 mg/lb one time daily. Treatment should be continued 24 hours following remission of disease signs, not to exceed 5 days. Do not inject more than 10 mL per site.

Vaccine Precautions:

Do not use Titanium® BRSV 3, Titanium® 3 LP, Titanium® 3, Titanium® IBR LP, and Titanium® IBR in pregnant cows or in calves nursing pregnant cows. Abortions may result.

¹Elanco Animal Health. Data on File.

²Elanco Animal Health. Data on File.

³Elanco Animal Health. Data on File.

⁴Milliken, G. A. 2013. Mannheimia haemolytica efficacy studies demonstrating the absence of excessive interference of Titanium products with the Mannheimia haemolytica-Pasteurella multocida bacterin-toxoid.

Full Value Beef, Component, Compudose, Encore, Micotil, Optaflexx, Pulmotil, Rumensin, StandGuard, Tylan, Titanium and Benchmark are trademarks of Elanco or its affiliates.