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