BMD Soluble Powder

ZOETIS INC.
333 PORTAGE STREET, KALAMAZOO, MI, 49007
Telephone: 269-359-4414
Customer Service: 888-963-8471
Website: www.zoetis.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.
BMD® Soluble

Zoetis

(bacitracin methylenedisalicylate soluble powder)

For poultry and livestock drinking water

Broiler and replacement chickens

An aid in prevention and control of necrotic enteritis caused by Clostridium perfringens susceptible to bacitracin methylenedisalicylate.

Growing turkeys

An aid in control of transmissible enteritis (blue comb, mud fever) in growing turkeys complicated by organisms susceptible to bacitracin methylenedisalicylate.

Growing quail

For the prevention of ulcerative enteritis due to Clostridium colinum susceptible to bacitracin methylenedisalicylate.

Swine

For use in the treatment of swine dysentery associated with Brachyspira hyodysenteriae.

Active ingredient

Contains 51.2 g bacitracin activity from bacitracin methylenedisalicylate equivalent to 200 g bacitracin activity per pound or to 18,520 units bacitracin (master standard) per gram.

Ingredients

Granulated sugar, sodium bicarbonate, anti-caking agent.

Directions for use

Animal

Condition

Prevention

Control

Broiler and replacement chickens

Necrotic enteritis caused by Clostridium perfringens susceptible to bacitracin methylenedisalicylate.

100 mg / gal

200 - 400 mg / gal

Growing turkeys

Transmissible enteritis (blue comb, mud fever) complicated by organisms susceptible to bacitracin methylenedisalicylate.

-

400 mg / gal

Growing quail

Ulcerative enteritis due to Clostridium colinum susceptible to bacitracin methylenedisalicylate.

400 mg / gal

-

Swine

Swine dysentery (bloody scours) associated with Brachyspira hyodysenteriae.

-

1000 mg / gal

Prepare a fresh solution daily and use as sole source of drinking water.

Mixing instructions

For Proportioners:

Select the treatment dosage. Set the proportioner at the desired delivery rate. To prepare the proportioner’s stock solution, place the indicated quantity of BMD Soluble in a 2-gallon container, fill with water and stir until dissolved.

For Tanks:

One package of BMD Soluble will medicate approximately 50 gallons of water at a dosage of 1000 mg/gallon.

Treatment dosage

PROPORTIONER SET AT:

PROPORTIONER SET AT:

1 ounce/gallon

2 ounces/gallon

100 mg/gal

1/2 pack

1/4 pack

200 mg/gal*

1 pack

1/2 pack

400 mg/gal

2 packs

1 pack

1000 mg/gal

5 packs

2-1/2 packs

* 200 mg/gallon is equivalent to about 100 g of feed grade BMD per ton of feed

To control an outbreak, start medication at first clinical signs of disease. Consult a diagnostic laboratory or veterinarian to determine the diagnosis and advice regarding the optimal level of drug. For necrotic enteritis in broiler and replacement chickens, administer continuously 5-7 days or as long as clinical signs persist, then reduce medication to prevention levels (100 mg/gal).

For transmissible enteritis in turkeys, administer continuously as long as clinical signs persist. For swine dysentery start medication at first signs of the disease or at time of exposure and administer continuously for 7 days or until signs of dysentery disappear. Treatment not to exceed 14 days.

CAUTION: Not for use in swine weighing more than 250 lb.

Caution: Not for human use.

Keep out of reach of children.

For oral use in animals only.

Concentrated

For water medicators.

Store between 20°C - 25°C (68°F - 77°F); excursions permitted between 15°C - 37°C (59°F - 99°F).

Restricted Drug (California) - Use only as directed.

Approved by FDA under NADA # 065-470

Distributed by:

Zoetis Inc., Kalamazoo, MI 49007

Net Weight



4.1 oz (116.2 g) Proportioner Pack

40040477

CPN: 3690446.3COLORADO 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