NDC 86241-101 - Ozipco

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 86241-101
Package NDCs from labels: 86241-101-01
Manufacturer: Fast Sold LLC | Zhejiang Hisun Pharmaceutical Co., Ltd.
Effective date: 2026-09-18
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ozipco ® (fenbendazole)	Fast Sold LLC \| Zhejiang Hisun Pharmaceutical Co., Ltd.	2026-09-18	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
86241-101-01	Ozipco	1 in 1 CARTON	PASTE	1		1
86241-101-01	Ozipco	25 g in 1 SYRINGE, PLASTIC	PASTE	25		1

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 unii: 621BVT9M36

Reported adverse events (FAERS/openFDA)#

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