| Product NDC: | 42192-134 |
| Proprietary Name: | Salicylic Acid |
| Non Proprietary Name: | SALICYLIC ACID |
| Active Ingredient(s): | 60 mg/g & nbsp; SALICYLIC ACID |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 42192-134 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110519 |
| Package NDC: | 42192-134-40 |
| Package Description: | 1 TUBE in 1 CARTON (42192-134-40) > 40 g in 1 TUBE |
| NDC Code | 42192-134-40 |
| Proprietary Name | Salicylic Acid |
| Package Description | 1 TUBE in 1 CARTON (42192-134-40) > 40 g in 1 TUBE |
| Product NDC | 42192-134 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SALICYLIC ACID |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110519 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | SALICYLIC ACID |
| Strength Number | 60 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |