FENBENPRO

Manufacturer: HUBIHOL, UAB
Effective date: 2025-01-28
Label type: OTC ANIMAL DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:44:16

Label at a glance#

ProductFENBENPRO

Active ingredientFENBENDAZOLE

Label structure2 sections

Contacts and useful links#

Websitewww.fenben.pro

www.fenben.pro/msds

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients
Fenbendazole 99.95%

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts
Active Ingredients
FENBENPRO
PURITY & PRECISION
FENBENDAZOLE
Laboratory tested | Purity > 99,95%
Fenbendazole 99.95% (100g)
100gr/3.5oz | Powder
Purpose Dewormer for Pets Only Uses • For the treatment and control of Roundworms (Toxocara canis, Toxascaris leonina), • Hookworms (Ancylostoma caninum, Uncinaria stenocephala), • Whipworms (Trichuris vulpis) •Tapeworms (Taenia pisiformis).
Warnings
Keep out of reach of children if swallowed get medical help or contact a Poison Control Centre right away. Do not deworm a pet that is sick. Consult your veterinarian for assistance in the diagnosis, treatment and control of parasitism.
Directions You should weigh your pet to make sure you are using the right dose.
Pet weight
10 lbs
20 lbs
30 lbs
Daily dose
227mg
450mg
680mg
Lot Number: F24/05-07 Best Use Before: 2027/05
CAS No: 43210-67-9
Molecular formula: C1H12N2O,S
15 13 3
2
Molecular weight: 299.35 Contains a silica gel packet to prevent moisture. Store in a cool, dry place away from direct sunlight. Keep out of reach of children.
Safety data sheet available at: www.fenben.pro/msds
9
69168 3495 2
1
FEN-100-POW
Distributed by
Hubihol LTD Lithuania Laboratory institute
Structural formula
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Content of Labeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
86217-0003-1	FENBENPRO	100 g in 1 PACKAGE	POWDER	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
86217-0003	FENBENPRO POWDER [HUBIHOL, UAB]	1	1 package rows	20250130_19b80438-095b-4fe7-a763-35873bcdbe2b.zip

Products#

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

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

FENBENPRO
FENBENDAZOLE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
86217-0003	86217-0003-1

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
Name	UNII	Kind
FENBENDAZOLE	621BVT9M36	ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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