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NeoBenz Micro Plus Pack - 67402-021-23 - (benzoyl peroxide)

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Drug Information of NeoBenz Micro Plus Pack

Product NDC: 67402-021
Proprietary Name: NeoBenz Micro Plus Pack
Non Proprietary Name: benzoyl peroxide
Active Ingredient(s):    & nbsp;   benzoyl peroxide
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of NeoBenz Micro Plus Pack

Product NDC: 67402-021
Labeler Name: SkinMedica Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20090416

Package Information of NeoBenz Micro Plus Pack

Package NDC: 67402-021-23
Package Description: 1 KIT in 1 BOX (67402-021-23) * 45 g in 1 TUBE * 7 POUCH in 1 CASE (67402-023-07) > .5 g in 1 POUCH (67402-023-01)

NDC Information of NeoBenz Micro Plus Pack

NDC Code 67402-021-23
Proprietary Name NeoBenz Micro Plus Pack
Package Description 1 KIT in 1 BOX (67402-021-23) * 45 g in 1 TUBE * 7 POUCH in 1 CASE (67402-023-07) > .5 g in 1 POUCH (67402-023-01)
Product NDC 67402-021
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzoyl peroxide
Dosage Form Name KIT
Route Name
Start Marketing Date 20090416
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name SkinMedica Pharmaceuticals, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of NeoBenz Micro Plus Pack


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