| Product NDC: | 51439-007 |
| Proprietary Name: | Acne Clearning Treatment |
| Non Proprietary Name: | SULFUR, BENZOYL PEROXIDE, SALICYLIC ACID |
| Active Ingredient(s): | .006; .0048; .012 mg/.024mg; mg/.024mg; mg/.024mg & nbsp; SULFUR, BENZOYL PEROXIDE, SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51439-007 |
| 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: | 51439-007-02 |
| Package Description: | 3 BOTTLE in 1 BOX (51439-007-02) > .024 mg in 1 BOTTLE (51439-007-01) |
| NDC Code | 51439-007-02 |
| Proprietary Name | Acne Clearning Treatment |
| Package Description | 3 BOTTLE in 1 BOX (51439-007-02) > .024 mg in 1 BOTTLE (51439-007-01) |
| Product NDC | 51439-007 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULFUR, BENZOYL PEROXIDE, SALICYLIC ACID |
| 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; SALICYLIC ACID; SULFUR |
| Strength Number | .006; .0048; .012 |
| Strength Unit | mg/.024mg; mg/.024mg; mg/.024mg |
| Pharmaceutical Classes |