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Bengay Ultra Strength - 58232-6001-4 - (Menthol)

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Drug Information of Bengay Ultra Strength

Product NDC: 58232-6001
Proprietary Name: Bengay Ultra Strength
Non Proprietary Name: Menthol
Active Ingredient(s): 50    mg/1 & nbsp;   Menthol
Administration Route(s): TOPICAL
Dosage Form(s): PATCH
Coding System: National Drug Codes(NDC)

Labeler Information of Bengay Ultra Strength

Product NDC: 58232-6001
Labeler Name: JJohnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120901

Package Information of Bengay Ultra Strength

Package NDC: 58232-6001-4
Package Description: 4 POUCH in 1 CARTON (58232-6001-4) > 1 PATCH in 1 POUCH

NDC Information of Bengay Ultra Strength

NDC Code 58232-6001-4
Proprietary Name Bengay Ultra Strength
Package Description 4 POUCH in 1 CARTON (58232-6001-4) > 1 PATCH in 1 POUCH
Product NDC 58232-6001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Menthol
Dosage Form Name PATCH
Route Name TOPICAL
Start Marketing Date 20120901
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name JJohnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance Name MENTHOL
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Bengay Ultra Strength


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