| Product NDC: | 59779-807 |
| Proprietary Name: | CVS Triple Action Astringent |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 20.5 mg/mL & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59779-807 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100708 |
| Package NDC: | 59779-807-62 |
| Package Description: | 250 mL in 1 BOTTLE, PLASTIC (59779-807-62) |
| NDC Code | 59779-807-62 |
| Proprietary Name | CVS Triple Action Astringent |
| Package Description | 250 mL in 1 BOTTLE, PLASTIC (59779-807-62) |
| Product NDC | 59779-807 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100708 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | SALICYLIC ACID |
| Strength Number | 20.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |