BenzEFoam - 16781-194-96 - (BENZOYL PEROXIDE)

Alphabetical Index


Drug Information of BenzEFoam

Product NDC: 16781-194
Proprietary Name: BenzEFoam
Non Proprietary Name: BENZOYL PEROXIDE
Active Ingredient(s): 5.3    g/100g & nbsp;   BENZOYL PEROXIDE
Administration Route(s): TOPICAL
Dosage Form(s): AEROSOL, FOAM
Coding System: National Drug Codes(NDC)

Labeler Information of BenzEFoam

Product NDC: 16781-194
Labeler Name: Onset Dermatologics LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090918

Package Information of BenzEFoam

Package NDC: 16781-194-96
Package Description: 1 CAN in 1 BOX (16781-194-96) > 100 g in 1 CAN

NDC Information of BenzEFoam

NDC Code 16781-194-96
Proprietary Name BenzEFoam
Package Description 1 CAN in 1 BOX (16781-194-96) > 100 g in 1 CAN
Product NDC 16781-194
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BENZOYL PEROXIDE
Dosage Form Name AEROSOL, FOAM
Route Name TOPICAL
Start Marketing Date 20090918
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Onset Dermatologics LLC
Substance Name BENZOYL PEROXIDE
Strength Number 5.3
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of BenzEFoam


General Information