AcneWorx - 28109-010-06 - (salicylic acid)

Alphabetical Index


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

Complete Information of AcneWorx


General Information