Liquamycin LA-200 is a long-lasting, broad-spectrum antibiotic containing 200 mg oxytetracycline per ml. LA-200 is effective in the treatment of a wide range of diseases, including pinkeye, footrot, and pneumonia. For use in beef cattle, dairy cattle, calves, and swine. Approved for 96 hour milkout. LA-200 provides therapeutic levels of oxytetracycline in the blood for 3 days. Most animals show a noticeable improvement within 24 to 48 hours. Give 4.5 ml per 100 pounds intramuscular or subcutaneous in neck. Oxytetracycline.
Liquamycin LA-200 is a sterile, preconstituted solution of the broad-spectrum antibiotic oxytetracycline. Each mL contains 200 mg of oxytetracycline base as oxytetracycline dihydrate, and on a w/v basis, 40.0% 2-pyrrolidone, 5.0% povidone, 1.8% magnesium oxide, 0.2% sodium formaldehyde sulfoxylate (as a preservative), monoethanolamine and/or hydrochloric acid as required to adjust pH.
Broad-spectrum antibiotic for the treatment in cattle and swine for various upper respiratory and general infections. Sterile, ready-to-use, broad-spectrum antibiotic for use in beef cattle, dairy cattle, calves including preruminating (veal) calves, and swine. Approved for use in lactating dairy cows. Effective in treating a wide range of diseases caused by susceptible gram-positive and gram-negative bacteria including pinkeye, pneumonia, shipping fever, foot rot, diphtheria, bacterial scours, metritis, wound infections, leptospirosis (L. Pomona) and wooden tongue.
Indicated in the treatment of pneumonia and shipping fever complex associated with Pasteurella spp. and Haemophilus spp.; infectious bovine keratoconjunctivitis (pinkeye) caused by Moraxella bovis; foot rot and diphtheria caused by Fusobacterium necrophorum; bacterial enteritis (scours) caused by Escherichia coli (E. coli); wooden tongue caused by Actinobacillus lignieresii; leptospirosis caused by Leptospira interrogans serovar pomona; and wound infections and acute metritis caused by strains of staphylococci and streptococci organisms sensitive to oxytetracycline.
Cattle dosage: 4.5 ml intramuscularly or subcutaneously per 100 lbs body weight.
Swine dosage: 4.5 ml intramuscularly per 100 lbs body weight.
Do not administer more than 10 ml at any one injection site.
Caution: When administered to cattle, muscle discoloration may necessitate trimming of the injection site(s) and surrounding tissues during the dressing procedure.
Warnings: Discontinue treatment at least 28 days prior to slaughter of cattle and swine. Milk taken from animals during treatment and for 96 hours after the last treatment must not be used for food.
Precautions: Exceeding the highest recommended level of drug per pound of body weight per day, administering more than the recommended number of treatments, and/or exceeding 10 mL subcutaneously per injection site in adult beef and dairy cattle, and 5 mL intramuscularly per injection site in adult swine, may result in antibiotic residues beyond the withdrawal period.
Discontinue treatment with LIQUAMYCIN LA-200 at least 28 days prior to slaughter. Discard milk for 96 hours after the last treatment. Do not exceed the highest recommended level of drug per pound of body weight per day.
Manufacturer and/or Label Information
Manufacturer and/or Label Information
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
Contact us for information on other Colorado Serum Company products. Fine Veterinary Products since 1923.
FOR VETERINARY USE ONLY
10 - 1 ml vials
10 - 1 dose vials