Prohibit Soluble Drench Dewormer for Cattle and Sheep (52 gram)

HUVEPHARMA, INC.
525 WESTPARK DR., SUITE 230, PEACHTREE CITY, GA, 30269
Telephone: 770-486-7212
Toll-Free: 877-994-4883
Fax: 770-486-7217
Website: www.huvepharma.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.
PROHIBIT® SOLUBLE DRENCH POWDER

Huvepharma

(levamisole hydrochloride)

Anthelmintic

Each packet contains 46.8 g of levamisole hydrochloride activity.

Each bottle contains 544.5 g of levamisole hydrochloride activity.

NOT FOR USE IN HUMANS

KEEP OUT OF REACH OF CHILDREN

Restricted Drug (California) - Use Only as Directed

Approved by FDA under ANADA # 200-225

CATTLE AND SHEEP DEWORMER FOR ORAL USE

Administer as a standard drench with standard drench syringe or administer as a concentrated drench solution with an automatic drenching syringe.

INDICATIONS:

Prohibit (levamisole hydrochloride) is a broad-spectrum anthelmintic and is effect against the following nematode infections in cattle and sheep:

SHEEP:

STOMACH WORMS: Haemonchus contortus, Trichostrongylus axei, Teladorsagia circumcincta.

INTESTINAL WORMS: Trichostrongylus colubriformis, Cooperia curticei, Nematodirus spathiger, Bunostomum trigonocephalum, Oesophagostomum columbianum, Chabertia ovina.

LUNGWORMS: Dictyocaulus filaria.

CATTLE:

STOMACH WORMS: Haemonchus placei, Trichostrongylus axei, Ostertagia ostertagi.

INTESTINAL WORMS: Trichostrongylus longispicularis, Cooperia oncophora, Cooperia punctata, Nematodirus spathiger, Bunostomum phlebotomum, Oesophagostomum radiatum.

LUNGWORMS: Dictyocaulus viviparus.

DOSAGE AND ADMINISTRATION

Packet - CATTLE-STANDARD DRENCH SOLUTION: Place the contents of packet in a 1 quart (32 fl oz) container, fill with water; swirl until dissolved. Administer as a single drench dose according to the following table:

Weight

Drench Dosage

Packet Will Treat

200 lb.

1/2 fl. oz.

64 head

400 lb.

1 fl. oz.

32 head

600 lb.

1 1/2 fl. oz.

21 head

800 lb.

2 fl. oz.

16 head

CONCENTRATED DRENCH SOLUTION: For use with automatic syringe. Place the contents of packet in a standard household measuring container and add water to the 8 3/4 fl. oz. level; or use the measuring container available from your supplier and add water to the mark. Swirl until dissolved. Give 2 ml (milliliter) per 100 lb. body weight. Refer to the table above for the number of cattle this packet will treat.

SHEEP-STANDARD DRENCH SOLUTION: Place the contents of packet in a 1 gallon (128 fl. oz.) container, fill with water; swirl until dissolved. Administer as a single drench dose according to the following table:

Weight

Drench Dosage

Packet Will Treat

50 lb.

1/2 fl. oz.

256 head

100 lb.

1 fl. oz.

128 head

150 lb.

1 1/2 fl. oz.

84 head

200 lb.

2 fl. oz.

64 head

CONCENTRATED DRENCH SOLUTION: Packet - For use with automatic syringe. Place the contents of packet in a standard household measuring container and add water to the 17 1/2 fl. oz. level. Swirl until dissolved. Give 2 ml per 50 lb. body weight. Refer to the table above for the number of sheep this packet will treat.

DOSAGE AND ADMINISTRATION: Bottle - When you are ready to deworm your cattle or sheep, add water to the powder in the bottle up to the 3 liter mark. Swirl to mix thoroughly before using. If any solution is left over, it may be stored for up to 3 months in this tightly capped bottle, shake well before using.

DATE WATER WAS ADDED TO THE BOTTLE

Month Day Year

Administer as a single drench dose as follows:

Cattle--2 mL per 100 lb. body weight

Weight

Drench Dosage

Bottle Will Treat

100 lb.

2 mL

1,500 head

300 lb.

6 mL

500 head

500 lb.

10 mL

300 head

700 lb.

14 mL

214 head

1,000 lb.

20 mL

150 head

Sheep--1 mL per 50 lb. body weight

Weight

Drench Dosage

Bottle Will Treat

50 lb.

1 mL

3,000 head

100 lb.

2 mL

1,500 head

150 lb.

3 mL

1,000 head

200 lb.

4 mL

750 head

Do not underdose. Ensure each animal receives a complete dose based on a current body weight. Underdosing may result in ineffective treatment, and encourage the development of parasite resistance.

NOTE: Careful weight estimates are essential for proper performance of this product. Prepare solutions as needed. However, excess solutions may be stored in clean closed containers up to 90 days without loss of anthelmintic activity. Cattle and Sheep maintained under conditions of constant helminth exposure may require re-treatment within two to four weeks after the first treatment.


RESIDUE WARNING: Do not administer to cattle within 48 hours of slaughter for food. Do not administer to sheep within 72 hours of slaughter for food. To prevent residues in milk, do not administer to dairy animals of breeding age.


OTHER WARNINGS: Parasite resistance may develop to any dewormer, and has been reported for most classes of dewormers. Treatment with a dewormer used in conjunction with parasite management practices appropriate to the geographic area and the animal(s) to be treated may slow the development of parasite resistance. Fecal examinations or other diagnostic tests and parasite management history should be used to determine if the product is appropriate for the herd/flock, prior to the use of any dewormer. Following the use of any dewormer, effectiveness of treatment should be monitored (for example, with the use of a fecal egg count reduction test or another appropriate method). A decrease in a drug’s effectiveness over time as calculated by fecal egg count reduction tests may indicate the development of resistance to the dewormer administered. Your parasite management plan should be adjusted accordingly based on regular monitoring.

CAUTION: Muzzle foam may be observed. However, this reaction will disappear within a few hours. If this condition persists, a veterinarian should be consulted. Follow recommended dosage carefully. Consult veterinarian before using in severely debilitated animals.

Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.

To report suspected adverse drug events, for technical assistance or to obtain a copy of the Safety Data Sheet (SDS), contact Huvepharma, Inc. at 1-877-994-4883 or www.huvepharma.us. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae.

Store between 20°-25°C (68°-77°F).

HOW SUPPLIED: 52 g (1.8 oz) and 605 g (21.34 oz)

Manufactured for Huvepharma, Inc., Peachtree City, GA 30269

® Registered Trademark of Huvepharma, Inc.



NDC





NET WEIGHT: 1.8 oz (52 g)

23243-2320-5

MF: L-6232-05

Rev: 03-2022

Net Contents: 15 x 1.8 oz (52 g) Pouches





Rev. 03-2022

Net Contents: 30 x 1.8 oz (52 g)

23243-2320-5

MF# L-6232-05

Rev. 03-2022

Net Wt: 21.34 oz. (1.3 lb.) (605 g)

23243-2320-6

MF# L-6232-60

Rev. 03-2022

CPN: 1309078.0

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