MaxClarity - 0145-2832-09 - (benzoyl peroxide)

Alphabetical Index


Drug Information of MaxClarity

Product NDC: 0145-2832
Proprietary Name: MaxClarity
Non Proprietary Name: benzoyl peroxide
Active Ingredient(s): 25    mg/g & nbsp;   benzoyl peroxide
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of MaxClarity

Product NDC: 0145-2832
Labeler Name: Stiefel Laboratories Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110622

Package Information of MaxClarity

Package NDC: 0145-2832-09
Package Description: 1 TUBE in 1 CARTON (0145-2832-09) > 156 g in 1 TUBE

NDC Information of MaxClarity

NDC Code 0145-2832-09
Proprietary Name MaxClarity
Package Description 1 TUBE in 1 CARTON (0145-2832-09) > 156 g in 1 TUBE
Product NDC 0145-2832
Product Type Name HUMAN OTC DRUG
Non Proprietary Name benzoyl peroxide
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20110622
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Stiefel Laboratories Inc
Substance Name BENZOYL PEROXIDE
Strength Number 25
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of MaxClarity


General Information