Fenbendazole 222 MG

Manufacturer: B & L Healthcare Products INC
Effective date: 2025-04-23
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:59:40

Label at a glance#

ProductFenbendazole 222 MG

Active ingredientFENBENDAZOLE

Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Febendazole

INACTIVE INGREDIENT SECTION

Ivermectin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTHER SAFETY INFORMATION

Keep in a cool, dry place and avoid sunlight.

DOSAGE & ADMINISTRATION SECTION

2 capsules per day

OTC - PURPOSE SECTION

Dewormer

WARNINGS SECTION

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 SECTION

Dewormer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

fenbendazole

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
7fd951fe-040a-0b64-2bea-eefc6aa4fc54	Product name	2	20250515
5b0ed980-56ce-7dd0-fb86-ff54be67c2e6	Product name	2	20200925
eed31638-1288-4eb6-a55c-5fc014dca98d	Product name	3	20200728

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
85130-100-01	Fenbendazole 222 MG	120 in 1 BOTTLE, PLASTIC	CAPSULE	120	1
85130-100-01	Fenbendazole 222 MG	222 mol in 1 CAPSULE	CAPSULE	222	1
85130-100-02	Fenbendazole 222 MG	90 in 1 BOTTLE, PLASTIC	CAPSULE	90	1
85130-100-02	Fenbendazole 222 MG	444 mol in 1 CAPSULE	CAPSULE	444	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
85130-100	FENBENDAZOLE 222 MG CAPSULE [B & L HEALTHCARE PRODUCTS INC]	1	Current NDC, 4 package rows	20250426_337c4554-2049-a725-e063-6394a90a66f5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Fenbendazole 222 MG
FENBENDAZOLE
IVERMECTIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85130-100	85130-100-01, 85130-100-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
FENBENDAZOLE	621BVT9M36	ACTIB
IVERMECTIN	8883YP2R6D	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fenbendazole 222 MG	FENBENDAZOLE 222 MG	B & L Healthcare Products INC	337c4554-2049-a725-e063-6394a90a66f5	2025-04-23	Warnings	Exact identifier ndc (package): 85130-100-02 ndc (package): 85130-100-01 ndc (product): 85130-100 ndc11 (package): 85130010001 ndc11 (package): 85130010002 spl id: 337c4554-204a-a725-e063-6394a90a66f5 spl set id: 337c4554-2049-a725-e063-6394a90a66f5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.