| Product NDC: | 54726-0100 |
| Proprietary Name: | St. Ives Blemish and Blackhead control |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | .02 g/g & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54726-0100 |
| Labeler Name: | Cosmetic Laboratories of America |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110223 |
| Package NDC: | 54726-0100-7 |
| Package Description: | 212 g in 1 TUBE (54726-0100-7) |
| NDC Code | 54726-0100-7 |
| Proprietary Name | St. Ives Blemish and Blackhead control |
| Package Description | 212 g in 1 TUBE (54726-0100-7) |
| Product NDC | 54726-0100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110223 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cosmetic Laboratories of America |
| Substance Name | SALICYLIC ACID |
| Strength Number | .02 |
| Strength Unit | g/g |
| Pharmaceutical Classes |