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BENZOYL PEROXIDE - 49035-021-13 - (BENZOYL PEROXIDE)

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Drug Information of BENZOYL PEROXIDE

Product NDC: 49035-021
Proprietary Name: BENZOYL PEROXIDE
Non Proprietary Name: BENZOYL PEROXIDE
Active Ingredient(s):    & nbsp;   BENZOYL PEROXIDE
Administration Route(s): TOPICAL
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of BENZOYL PEROXIDE

Product NDC: 49035-021
Labeler Name: Wal-Mart Stores Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100226

Package Information of BENZOYL PEROXIDE

Package NDC: 49035-021-13
Package Description: 1 KIT in 1 KIT (49035-021-13) * 120 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC

NDC Information of BENZOYL PEROXIDE

NDC Code 49035-021-13
Proprietary Name BENZOYL PEROXIDE
Package Description 1 KIT in 1 KIT (49035-021-13) * 120 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC
Product NDC 49035-021
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZOYL PEROXIDE
Dosage Form Name KIT
Route Name TOPICAL
Start Marketing Date 20100226
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Wal-Mart Stores Inc
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of BENZOYL PEROXIDE


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