Product NDC: | 28109-010 |
Proprietary Name: | AcneWorx |
Non Proprietary Name: | salicylic acid |
Active Ingredient(s): | .6 g/30mL & nbsp; salicylic acid |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 28109-010 |
Labeler Name: | DermWorx Incorporated |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080114 |
Package NDC: | 28109-010-06 |
Package Description: | 6 CARTON in 1 CARTON (28109-010-06) > 1 TUBE in 1 CARTON (28109-010-01) > 30 mL in 1 TUBE |
NDC Code | 28109-010-06 |
Proprietary Name | AcneWorx |
Package Description | 6 CARTON in 1 CARTON (28109-010-06) > 1 TUBE in 1 CARTON (28109-010-01) > 30 mL in 1 TUBE |
Product NDC | 28109-010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | salicylic acid |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20080114 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | DermWorx Incorporated |
Substance Name | SALICYLIC ACID |
Strength Number | .6 |
Strength Unit | g/30mL |
Pharmaceutical Classes |