PHENBENDAZOLE

Manufacturer
AMBIENCE FAMILY INC
Effective date
2024-05-01
Label type
OTC ANIMAL DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:43:07

Label at a glance#

ProductPHENBENDAZOLE
Active ingredientfenbendazole
Label structure4 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

Contains a silica gel packet inside to avoid moisture.
Keep in cool, dry place and avoid sun light.
Keep out of the reach of children.

SPL UNCLASSIFIED SECTION

CAS No:43210-67-9
Molecular formula:C15H13N3O2S
Molecular weight:299.35

DISTRIBUTED BY:
Hopaner Crest INC
United States
3717 Metro pkwy
Unit 3108
FL FORT MYERS
33916

WARNINGS AND PRECAUTIONS SECTION

Not for use in humans. Keep out of reach of children. Protective gloves should be used and care should be taken when handling the product to avoid skin and eye exposure and accidental ingestion. Accidental exposure may result in skin and eye irritation. Accidental ingestion may cause gastrointestinal disturbances and hypersensitivity reactions in humans.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Laboratory tested·Purity >99%

Contains: >99% fenbendazole
Lot number: F19/1-05Content of LabelingContent of Labeling
Warranty: 2 years

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86202-3107-1PHENBENDAZOLE1.85 g in 1 CAPSULETABLET1.851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86202-3107PHENBENDAZOLE TABLET [AMBIENCE FAMILY INC]11 package rows20240524_d371478f-d352-4eda-ad23-a63fd08c907b.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86202-310786202-3107-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
fenbendazole621BVT9M36ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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