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Merck Animal Health

Bovilis Piliguard Pinkeye

Bovilis Piliguard Pinkeye

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For vaccination of healthy cattle to aid in the control of Pinkeye associated with infection by Moraxella bovis strains expressing pili similar to those expressed by isolates referred to as strains EPP63, FLA64 and SAH38.

Dosage: 2 ml IM or subcut in the neck 3-6 weeks prior to onset of pinkeye season. Annual revaccination is recommended. 60 day slaughter withdrawal. 

Anaphylactoid reactions may occur. Antidote : Epinephrine.



Manufacturer and/or Label Information

MERCK ANIMAL HEALTH
Intervet Inc.
126 E. LINCOLN AVENUE, PO BOX 2000, Rahway, NJ, 07065
Customer Service: 800-521-5767
Technical Service (Companion Animal): 800-224-5318
Technical Service (Livestock): 800-211-3573
Website: www.merck-animal-health-usa.com
THIS SERVICE AND DATA ARE PROVIDED "AS IS". DVMetrics assumes no liability, and each user assumes full risk, responsibility, and liability, related to its use of the DVMetrics service and data. See the Terms of Use for further details.
BOVILIS® Piliguard® Pinkeye

Intervet/Merck Animal Health

Moraxella Bovis Bacterin

This product has been shown effective for the vaccination of healthy cattle against Moraxella bovis. This product was licensed prior to the requirement to establish minimum age for use. Duration of immunity has not been established. For more information regarding efficacy and safety data, go to productdata.aphis.usda.gov.

ADMINISTRATION: The vaccine may be warmed to room temperature prior to injection. Shake well and using aseptic technique inject 2.0 mL dose intramuscularly or subcutaneously into the neck 3-6 weeks prior to onset of pinkeye season. Historically, annual revaccination with this product has been recommended. The need for this booster has not been established. For more information on revaccination frequency, consult your veterinarian.

CAUTION: Store at 2°-8°C (35°-46°F). Do not freeze. Use entire contents when first opened. Do not mix with other products. Do not vaccinate within 60 days before slaughter. Use may occasionally lead to development of granulomas which may persist for several weeks. Transient local reaction may occur at the injection site. This product has not been tested in pregnant animals. If allergic reaction occurs, treat with epinephrine. Extreme caution should be used with any oil emulsion vaccine; avoid injecting your own finger or hand. Accidental injection can cause serious local reaction. In case of human exposure, contact a physician. Contains Gentamicin and Formaldehyde as preservatives.

FOR ANIMAL USE ONLY

Intervet Inc., d/b/a Merck Animal Health, Omaha, NE 68103 USA

VLN 165A/PCN 2772.03

1 800 521-5767

For patent information: http://www.merck.com/product/patent/home.html







Code



20 mL

10 Doses

2 mL per dose

065410

346603-18

100 mL

50 Doses

143130

355805-02

CPN: 1047153.6



COLORADO SERUM COMPANY4950 YORK STREET, P.O. BOX 16428, DENVER, CO, 80216-0428Telephone: 303-295-7527Order Desk: 800-525-2065Fax: 303-295-1923Website: www.colorado-serum.comEmail: colorado-serum@colorado-serum.comTHIS SERVICE AND DATA ARE PROVIDED "AS IS". DVMetrics assumes no liability, and each user assumes full risk, responsibility, and liability, related to its use of the DVMetrics service and data. See the Terms of Use for further details.

TETANUS TOXOID-CONCENTRATED

Colorado Serum

Adjuvanted

GENERAL INFORMATION: This product has been shown to be effective for the vaccination of healthy horses, cattle, sheep, goats, and swine against tetanus. This product was licensed prior to the requirement to establish a minimum age for use. The duration of immunity is unknown. For more information regarding efficacy and safety data, see productdata.aphis.usda.gov.

Safety in pregnant animals is unknown.

Tetanus Toxoid is prepared by detoxifying tetanus toxin in such a manner as to allow the antigenic properties to remain intact. Product is purified, concentrated and adjuvanted to provide a low dose effective immunizing agent.

Each serial is tested for purity, safety, and potency in accordance with USDA requirements.

Tetanus is caused by a neurotoxin produced by growth of Clostridium tetani, an anaerobic (lives without air) micro-organism, in necrotic tissue. Affected animals become stiff, have difficulty swallowing, and have an increased pulse rate. Breathing is labored. Spasmodic contractions of the muscular system occur, such as contracting muscles of the jaw.

Spasmodic contractions of the muscular system occur, such as contracting muscles of the jaw. Thus, the term “lockjaw” is often used. Legs and tail are often stiff with abdominal muscles contracted. Tetanus stricken animals may be unusually sensitive to light and heat. Temperature of the animal generally remains normal, elevating only shortly before death.

Protective antibody levels usually occur about two weeks after the second injection of the primary immunization series. In contrast, administration of Tetanus Antitoxin is recommended for immediate, emergency, passive treatment of exposed animals with unknown vaccination history or with signs of tetanus infection.

DIRECTIONS: Do not vaccinate within 21 days before slaughter. Store at 2-8° C. Do not freeze. Do not mix with other products. Shake well before use. Use entire contents when first opened.

PRECAUTIONS: A transitory local reaction may occur at injection site. Anaphylactoid reaction may occur following administration of products of this nature. If noted, administer adrenalin or equivalent. In case of human exposure, consult a physician.

DOSAGE & ADMINISTRATION: For primary immunization, two doses should be administered subcutaneously or intramuscularly approximately 30 days apart. Use intramuscularly for horses as local reactions are more likely to occur if injected subcutaneously.

Horses: 1 ml IM

Cattle: 1 ml SC or IM

Sheep, Goats, Swine: 0.5 ml SC or IM

Historically, annual single dose revaccination has been recommended. Contact veterinarian for advice.

OTHER INFORMATION: Contains thimerosal and formalin as preservatives. Tetanus Toxoid Concentrate is available in single dose size packaged 10 vials to the carton, and in 10 dose vials.

THE PEAK OF QUALITY SINCE 1923

VLN: 188 / PCN: 8601.00

COLORADO SERUM COMPANY, 4950 York Street, Denver, Colorado 80216

303-295-752

www.colorado-serum.com

Contact us for information on other Colorado Serum Company products. Fine Veterinary Products since 1923.

FOR VETERINARY USE ONLY

 

 

Order #

10 - 1 ml vials

10 - 1 dose vials

11411

10 ml

10 doses

11415

CPN: 1101033.3

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