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Remedy Antifungal - 53329-162-04 - (Miconazole Nitrate)

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Drug Information of Remedy Antifungal

Product NDC: 53329-162
Proprietary Name: Remedy Antifungal
Non Proprietary Name: Miconazole Nitrate
Active Ingredient(s): 20    mg/g & nbsp;   Miconazole Nitrate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Remedy Antifungal

Product NDC: 53329-162
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333C
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070101

Package Information of Remedy Antifungal

Package NDC: 53329-162-04
Package Description: 113 g in 1 TUBE (53329-162-04)

NDC Information of Remedy Antifungal

NDC Code 53329-162-04
Proprietary Name Remedy Antifungal
Package Description 113 g in 1 TUBE (53329-162-04)
Product NDC 53329-162
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Miconazole Nitrate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20070101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Medline Industries, Inc.
Substance Name MICONAZOLE NITRATE
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Remedy Antifungal


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