Home > National Drug Code (NDC) > Bengay Ultra Strength Pain Relieving

Bengay Ultra Strength Pain Relieving - 58232-4024-3 - (Camphor (Synthetic), Menthol, and Methyl Salicylate)

Alphabetical Index


Drug Information of Bengay Ultra Strength Pain Relieving

Product NDC: 58232-4024
Proprietary Name: Bengay Ultra Strength Pain Relieving
Non Proprietary Name: Camphor (Synthetic), Menthol, and Methyl Salicylate
Active Ingredient(s): 40; 100; 300    mg/g; mg/g; mg/g & nbsp;   Camphor (Synthetic), Menthol, and Methyl Salicylate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Bengay Ultra Strength Pain Relieving

Product NDC: 58232-4024
Labeler Name: Johnson & 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: 20120807

Package Information of Bengay Ultra Strength Pain Relieving

Package NDC: 58232-4024-3
Package Description: 1 TUBE in 1 CARTON (58232-4024-3) > 57 g in 1 TUBE

NDC Information of Bengay Ultra Strength Pain Relieving

NDC Code 58232-4024-3
Proprietary Name Bengay Ultra Strength Pain Relieving
Package Description 1 TUBE in 1 CARTON (58232-4024-3) > 57 g in 1 TUBE
Product NDC 58232-4024
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Camphor (Synthetic), Menthol, and Methyl Salicylate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120807
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance Name CAMPHOR (SYNTHETIC); MENTHOL; METHYL SALICYLATE
Strength Number 40; 100; 300
Strength Unit mg/g; mg/g; mg/g
Pharmaceutical Classes

Complete Information of Bengay Ultra Strength Pain Relieving


General Information