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 |