Strongid C 2X Horse Dewormer

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.
Strongid® C 2X™

Zoetis

(pyrantel tartrate)

Type C Medicated Feed

Equine Anthelmintic

Medicated For Continuous Feeding

For the prevention of Strongylus vulgaris larval infestation in horses

For the control of the following parasites in horses:

Large Strongyles (adults): S. vulgaris, S. edentatus

Small Strongyles (adults and 4th-stage larvae): Cyathostomum spp., Cylicocyclus spp., Cylicostephanus spp., Cylicodontophorus spp., Poteriostomum spp., Triodontophorus spp.

PINWORMS (adults and 4th-stage larvae): Oxyuris equi

ASCARIDS (adults and 4th-stage larvae): Parascaris equorum

Active Drug Ingredient:

pyrantel tartrate

2.11% (9.6 g/lb)

Guaranteed Analysis:

Crude Protein, not less than

11.5%

Crude Fat, not less than

1.5%

Crude Fiber, not more than

22.0%

Ingredients:

Dehydrated Alfalfa Meal, Wheat Middlings, Cane Molasses, Mineral Oil, preserved with propionic acid.

Mixing and Feeding Directions

Strongid C 2X is to be administered on a continuous basis either as a top-dress or mixed in the horse’s daily grain ration at the rate of 1.2 mg pyrantel tartrate per lb of body weight daily. To achieve this dose, administer 0.5 oz of Strongid C 2X per 250 lb of body weight. (A Strongid C 2X measuring cup is enclosed.) Strongid C 2X should be administered for the entire period that the animal is at risk to internal parasites. Unprotected animals that have grazed may already have an established S. vulgaris larval infestation. Before administering Strongid C 2X, these animals should be treated with a therapeutic dose of a larvicidal product.

Foals may be administered Strongid C 2X as soon as consistent intake of grain mix is occurring. This is generally between 2-3 months of age.

Strongid C 2X may be used in mares at any stage of pregnancy or lactation. Stallion fertility is not affected by the use of Strongid C 2X.

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.

Top-Dress Directions

Body Weight (lb)

oz per Day of Strongid C 2X

250

0.5

500

1.0

750

1.5

1000

2.0

1250

2.5

(Measuring Cup Enclosed)

Medicated Grain Mix Directions

lb of Medicated Grain Mix per 100 lb of Body Weight

lb of Strongid C 2X

lb of Non medicated Feed

Concentration Grams/Ton

2.0

12.5

1987.5

120

1.5

16.5

1983.5

160

1.0

25.0

1975

240

0.5

50.0

1950

480

0.2

125.0

1875

1200

Caution: Consult your veterinarian before using in severely debilitated animals and for assistance in the diagnosis, treatment, and control of parasitism. Do not mix in feeds containing bentonite.

Warnings:

Other Warnings: Do not use in horses intended for human consumption. 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 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.

Restricted Drug (California) - use only as directed

Distributed by:

Zoetis Inc., Kalamazoo, MI 49007

Product of Mexico

Approved by FDA under NADA # 140-819

Net Weight:



10 lb (4.5 kg)

10005904

50 lb (22.6 kg)

10005803

CPN: 3690140.8COLORADO 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