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Oxy Maximum Action Spot Treatment - 10742-8301-1 - (benzoyl peroxide)

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Drug Information of Oxy Maximum Action Spot Treatment

Product NDC: 10742-8301
Proprietary Name: Oxy Maximum Action Spot Treatment
Non Proprietary Name: benzoyl peroxide
Active Ingredient(s): 100    mg/g & nbsp;   benzoyl peroxide
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Oxy Maximum Action Spot Treatment

Product NDC: 10742-8301
Labeler Name: The Mentholatum Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130115

Package Information of Oxy Maximum Action Spot Treatment

Package NDC: 10742-8301-1
Package Description: 1 TUBE in 1 CARTON (10742-8301-1) > 18.4 g in 1 TUBE

NDC Information of Oxy Maximum Action Spot Treatment

NDC Code 10742-8301-1
Proprietary Name Oxy Maximum Action Spot Treatment
Package Description 1 TUBE in 1 CARTON (10742-8301-1) > 18.4 g in 1 TUBE
Product NDC 10742-8301
Product Type Name HUMAN OTC DRUG
Non Proprietary Name benzoyl peroxide
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130115
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name The Mentholatum Company
Substance Name BENZOYL PEROXIDE
Strength Number 100
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Oxy Maximum Action Spot Treatment


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