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AcneWorx
AcneWorx - 28109-010-06 - (salicylic acid)
Drug Information of AcneWorx
| 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) |
Labeler Information of AcneWorx
| 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 Information of AcneWorx
| 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 Information of AcneWorx
| 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 |
