FENBENDAZOLE 222 MG capsule

Fenbendazole 222 MG by

Drug Labeling and Warnings

Fenbendazole 222 MG by is a Otc medication manufactured, distributed, or labeled by B & L Healthcare Products INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Febendazole

INACTIVE INGREDIENT

Ivermectin

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

OTHER SAFETY INFORMATION

Keep in a cool, dry place and avoid sunlight.

DOSAGE & ADMINISTRATION

2 capsules per day

PURPOSE

Dewormer

WARNINGS

These statements have not been evaluated by the Food and DrugAdministration.

This product is not intended to diagnose, treat, cure, or prevent any diseases.

INDICATIONS & USAGE

Dewormer

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FENBENDAZOLE 222 MG 
fenbendazole 222 mg capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85130-100
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
FENBENDAZOLE (UNII: 621BVT9M36) (FENBENDAZOLE - UNII:621BVT9M36)	FENBENDAZOLE	299.35 mg  in 1 mol

Inactive Ingredients
Ingredient Name	Strength
IVERMECTIN (UNII: 8883YP2R6D)	12 mg  in 1 mol

Product Characteristics
Color	white	Score	no score
Shape	CAPSULE	Size	5mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85130-100-01	120 in 1 BOTTLE, PLASTIC	01/01/2015
1		222 mol in 1 CAPSULE; Type 0: Not a Combination Product
2	NDC: 85130-100-02	90 in 1 BOTTLE, PLASTIC	01/01/2015
2		444 mol in 1 CAPSULE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/01/2015

Labeler - B & L Healthcare Products INC (119398628)

Establishment
Name	Address	ID/FEI	Business Operations
B & L Healthcare Products INC		119398628	manufacture(85130-100)