Product NDC: | 59779-055 |
Proprietary Name: | CVS Acne Spot Treatment |
Non Proprietary Name: | SALICYLIC ACID |
Active Ingredient(s): | 20 mg/mL & nbsp; SALICYLIC ACID |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-055 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100710 |
Package NDC: | 59779-055-56 |
Package Description: | 1 TUBE in 1 CARTON (59779-055-56) > 22 mL in 1 TUBE |
NDC Code | 59779-055-56 |
Proprietary Name | CVS Acne Spot Treatment |
Package Description | 1 TUBE in 1 CARTON (59779-055-56) > 22 mL in 1 TUBE |
Product NDC | 59779-055 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SALICYLIC ACID |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20100710 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | SALICYLIC ACID |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes |