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Merck Animal Health

Safe-Guard Suspension 10% Dewormer for Cattle and Goats

Safe-Guard Suspension 10% Dewormer for Cattle and Goats

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For the removal and control of lungworms, stomach worms (adult and fourth stage larvae), brown stomach worms, intestinal worms (adult and fourth stage larvae), hookworms, thread-necked intestinal worms, small intestinal worms, bankrupt worms and nodular worms in cattle; stomach worms in goats. 

Contains 100 mg fenbendazole per ml.

•  Effective – Results prove 90% reduction in fecal egg counts*
•  Fast-acting – One day vs 7-14 days for competing dewormers*
•  Convenient – Administer chute-side or in the pasture
•  Proven – Shown to increase weaning weight by 28.9 lbs per head*

Dosage: Administer orally 2.3 ml per 100 lbs body weight. Each 1000 ml bottle will treat 86 - 500 lb animals or 430 - 100 lb animals.

Slaughter withdrawal: Cattle - 8 days; Goats - 6 days. Safe for lactating dairy cattle with no milk withholding. Withdrawal period has not been established in pre-ruminating calves. Do not use in veal calves or lactating goats.

Item cannot be shipped to California. 

Manufacturer and/or Label Information

MERCK ANIMAL HEALTH
Intervet Inc.
2 GIRALDA FARMS, MADISON, NJ, 07940
Customer Service: 800-521-5767
Order Desk: 800-648-2118
Technical Service (Companion Animal): 800-224-5318
Technical Service (Livestock): 800-211-3573
Fax: 973-937-5557
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.
safe-guard®

Intervet/Merck Animal Health

(fenbendazole)

Dewormer for Beef & Dairy Cattle and Goats

Suspension 10% (100 mg/mL)


Withdrawal Periods and Residue Warnings:

Milk taken from cows during treatment and for 48 hours after the last treatment must not be used for human consumption. Cattle must not be slaughtered for human consumption within 8 days following last treatment with this drug product. Not for use in beef calves less than 2 months of age, dairy calves, and veal calves. A withdrawal period has not been established for this product in pre-ruminating calves.

Goats must not be slaughtered for human consumption within 6 days following last treatment with this drug product. Because a milk discard time has not been established, do not use in lactating goats.


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

INDICATIONS:

Beef and Dairy Cattle - 2.3 mg/lb (5 mg/kg) body weight for the treatment and control of: Lungworms: Adult Dictyocaulus viviparus; Stomach worms: Adult brown stomach worms (Ostertagia ostertagi), Adult and fourth stage larvae barberpole worms (Haemonchus contortus & H. placei), and Adult and fourth stage larvae small stomach worms (Trichostrongylus axei); Intestinal worms (Adult and fourth stage larvae): hookworms (Bunostomum phlebotomum), thread-necked intestinal worms (Nematodirus helvetianus), small intestinal worms (Cooperia punctata & C. oncophora), bankrupt worms (Trichostrongylus colubriformis), and nodular worms (Oesophagostomum radiatum).

Goats - 2.3 mg/lb (5 mg/kg) body weight for the removal and control of:

Stomach worms (adults): Haemonchus contortus and Teladorsagia circumcincta.

DIRECTIONS: Administer orally. The recommended dose of 2.3 mg/lb (5 mg/kg) of body weight is achieved when 2.3 mL of the drug are given for each 100 lb body weight.

EXAMPLES:

Cattle:

Body Weight

Amount

100 lb

2.3 mL

200 lb

4.6 mL

300 lb

6.9 mL

400 lb

9.2 mL

500 lb

11.5 mL

1000 lb

23.0 mL

1500 lb

34.5 mL

Goats:

Body Weight

Amount

25 lb

0.6 mL

50 lb

1.2 mL

75 lb

1.7 mL

100 lb

2.3 mL

125 lb

2.9 mL

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.

WARNINGS: NOT FOR USE IN HUMANS. KEEP OUT OF REACH OF CHILDREN. The Safety Data Sheet (SDS) contains more detailed occupational safety information. For customer service, adverse effects reporting, and/or a copy of the SDS, call 1-800-211-3573. For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDAVETS, or http://www.fda.gov/reportanimalae.

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, 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.

Store at or below 25°C (77°F). Protect from freezing. Shake well before use. Restricted drug (California) - use only as directed.

Fenbendazole (active ingred.) made in China. Formulated in France.

Distributed by: Intervet Inc. (d/b/a Merck Animal Health), Madison, NJ 07940

Approved by FDA under NADA # 128-620

©2020 Intervet Inc., a subsidiary of Merck & Co. Inc.

1,000 mL (33.8 fl oz)

Rev. 11/20

361394 R9

385602 R10

1 Gallon (3,785 mL)

Rev. 09/20

386508 R4

367235 R3

10 Liter (338.1 fl oz)

Rev. 11/20

385311 R8

318203 R8

CPN: 1047396.3

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