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BenzEFoam Ultra - 16781-201-06 - (BENZOYL PEROXIDE)

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Drug Information of BenzEFoam Ultra

Product NDC: 16781-201
Proprietary Name: BenzEFoam Ultra
Non Proprietary Name: BENZOYL PEROXIDE
Active Ingredient(s): 9.8    g/100g & nbsp;   BENZOYL PEROXIDE
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of BenzEFoam Ultra

Product NDC: 16781-201
Labeler Name: Onset Dermatologics LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110304

Package Information of BenzEFoam Ultra

Package NDC: 16781-201-06
Package Description: 6 CAN in 1 CARTON (16781-201-06) > 5 g in 1 CAN

NDC Information of BenzEFoam Ultra

NDC Code 16781-201-06
Proprietary Name BenzEFoam Ultra
Package Description 6 CAN in 1 CARTON (16781-201-06) > 5 g in 1 CAN
Product NDC 16781-201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BENZOYL PEROXIDE
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20110304
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Onset Dermatologics LLC
Substance Name BENZOYL PEROXIDE
Strength Number 9.8
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of BenzEFoam Ultra


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