Cleanser - 51439-005-01 - (Benzoyl Peroxide)

Alphabetical Index


Drug Information of Cleanser

Product NDC: 51439-005
Proprietary Name: Cleanser
Non Proprietary Name: Benzoyl Peroxide
Active Ingredient(s): .006    mg/.024mg & nbsp;   Benzoyl Peroxide
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Cleanser

Product NDC: 51439-005
Labeler Name: CarePluss Pharma S.A. de C.V.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120806

Package Information of Cleanser

Package NDC: 51439-005-01
Package Description: .024 mg in 1 BOTTLE (51439-005-01)

NDC Information of Cleanser

NDC Code 51439-005-01
Proprietary Name Cleanser
Package Description .024 mg in 1 BOTTLE (51439-005-01)
Product NDC 51439-005
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzoyl Peroxide
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120806
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CarePluss Pharma S.A. de C.V.
Substance Name BENZOYL PEROXIDE
Strength Number .006
Strength Unit mg/.024mg
Pharmaceutical Classes

Complete Information of Cleanser


General Information