| Product NDC: | 76449-050 |
| Proprietary Name: | Blemish Control Blotting Paper |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | .03 mg/1 & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | STRIP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76449-050 |
| Labeler Name: | NYX Los Angeles Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part358H |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111215 |
| Package NDC: | 76449-050-01 |
| Package Description: | 100 STRIP in 1 PACKAGE (76449-050-01) |
| NDC Code | 76449-050-01 |
| Proprietary Name | Blemish Control Blotting Paper |
| Package Description | 100 STRIP in 1 PACKAGE (76449-050-01) |
| Product NDC | 76449-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | STRIP |
| Route Name | TOPICAL |
| Start Marketing Date | 20111215 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | NYX Los Angeles Inc. |
| Substance Name | SALICYLIC ACID |
| Strength Number | .03 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |