| 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 |