| 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: | 59779-807-31 | 
| Package Description: | 250 mL in 1 BOTTLE, PLASTIC (59779-807-31) | 
| NDC Code | 59779-807-31 | 
| Proprietary Name | CVS Triple Action Astringent | 
| Package Description | 250 mL in 1 BOTTLE, PLASTIC (59779-807-31) | 
| 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 |