OXY - 10742-8285-1 - (Salicylic acid)

Alphabetical Index


Drug Information of OXY

Product NDC: 10742-8285
Proprietary Name: OXY
Non Proprietary Name: Salicylic acid
Active Ingredient(s): 10    mg/mL & nbsp;   Salicylic acid
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of OXY

Product NDC: 10742-8285
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100802

Package Information of OXY

Package NDC: 10742-8285-1
Package Description: 295 mL in 1 BOTTLE (10742-8285-1)

NDC Information of OXY

NDC Code 10742-8285-1
Proprietary Name OXY
Package Description 295 mL in 1 BOTTLE (10742-8285-1)
Product NDC 10742-8285
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Salicylic acid
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20100802
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name The Mentholatum Company
Substance Name SALICYLIC ACID
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of OXY


General Information