NDC 79481-0621-01 - Anti-fungal Powder Miconazole Nitrate

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: 79481-0621
Requested NDC: 79481-0621-01
Package NDCs from labels: 79481-0621-1, 79481-0621-01
Manufacturer: Meijer Distribution Inc
Effective date: 2025-10-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Anti-fungal Powder Miconazole Nitrate - Meijer Distribution Inc	Meijer Distribution Inc	2025-10-31	HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79481-0621-1	Anti-fungal Powder Miconazole Nitrate	71 g in 1 BOTTLE, PLASTIC	POWDER	71		6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79481-0621	ANTI-FUNGAL POWDER MICONAZOLE NITRATE (MICONAZOLE NITRATE) POWDER [MEIJER DISTRIBUTION INC]	5	Current NDC, 1 package rows	20241016_03fd069d-685d-b8ac-e063-6394a90a31f8.zip

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 79 of 79 · 1,563 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Antimicrobial Hand Wash	CHLOROXYLENOL	Henry Schein, Inc.	5847a304-ff8e-4ae1-8bf0-ee7e6efb9451	2016-07-29	Warnings	Exact identifier unii: 0F32U78V2Q
Antimicrobial Hand Wash	CHLOROXYLENOL	Henry Schein, Inc.	a602672b-969e-44e1-821c-75aea6d063e7	2016-07-29	Warnings	Exact identifier unii: 0F32U78V2Q
Micatin	MICONAZOLE NITRATE	WellSpring Pharmaceutical Corporation	96c56ba1-c3a8-48ce-ab58-550959485e3c	2016-04-07	Warnings	Exact identifier application number: M005 unii: VW4H1CYW1K

Reported adverse events (FAERS/openFDA)#

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