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Safe-Guard

Schering Corporation

safe-guard (fenbendazole)


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Dewormer

for Goats

Suspension 10%
(100 mg/mL)

NOT FOR HUMAN USE

INDICATIONS

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

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

EXAMPLES:
Body Weight
Goats:
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

Under conditions of continued exposure to parasites, retreatment may be needed after 4 to 6 weeks.

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

RESIDUE WARNINGS

Goats must not be slaughtered for food within 6 days following treatment. Because a withdrawal time in milk has not been established, do not use in lactating goats.

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

Keep this and all medication out of the reach of children.

Made in France

Distributed by: Intervet Inc.
Millsboro, DE 19966
www.intervetusa.com

NADA # 128-620, Approved by FDA

PRINCIPAL DISPLAY PANEL - 125 ml Bottle Label

intervet

safe-guard ®
(fenbendazole)

Dewormer
for Goats

Suspension 10%
(100 mg/mL)

NOT FOR HUMAN USE

RESIDUE WARNINGS: Goats must
not be slaughtered for food within
6 days following treatment.
Because a withdrawal time in
milk has not been established,
do not use in lactating goats.

Consult your veterinarian for
assistance in the diagnosis, treat-
ment and control of parasitism.

Keep this and all medication
out of the reach of children.

125 mL (4.2 fl oz)

092310 LPFI240 01

Safe-Guard

Safe-Guard

Fenbendazole SUSPENSION

Product Information

Product Type Otc animal drug label Item Code (Source) NDC:57926-089
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Fenbendazole Fenbendazole 100 mg

Inactive Ingredients

Ingredient Name Strength
METHYLPARABEN
PROPYLPARABEN
SILICON DIOXIDE
CARBOXYMETHYLCELLULOSE SODIUM
POVIDONES
TRISODIUM CITRATE DIHYDRATE
CITRIC ACID MONOHYDRATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57926-089-01 125 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NADA NADA128620 2009-09-16


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Be sure to consult your doctor before taking any medication!
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