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OXY Clinical - 10742-8221-3 - (Salicylic acid)

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Drug Information of OXY Clinical

Product NDC: 10742-8221
Proprietary Name: OXY Clinical
Non Proprietary Name: Salicylic acid
Active Ingredient(s): 5    mg/g & nbsp;   Salicylic acid
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of OXY Clinical

Product NDC: 10742-8221
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100601

Package Information of OXY Clinical

Package NDC: 10742-8221-3
Package Description: 19.8 g in 1 TUBE (10742-8221-3)

NDC Information of OXY Clinical

NDC Code 10742-8221-3
Proprietary Name OXY Clinical
Package Description 19.8 g in 1 TUBE (10742-8221-3)
Product NDC 10742-8221
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Salicylic acid
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100601
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name The Mentholatum Company
Substance Name SALICYLIC ACID
Strength Number 5
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of OXY Clinical


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