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BPO 6 Foaming - 42192-125-60 - (BENZOYL PEROXIDE)

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Drug Information of BPO 6 Foaming

Product NDC: 42192-125
Proprietary Name: BPO 6 Foaming
Non Proprietary Name: BENZOYL PEROXIDE
Active Ingredient(s): 3.2    g/100g & nbsp;   BENZOYL PEROXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CLOTH
Coding System: National Drug Codes(NDC)

Labeler Information of BPO 6 Foaming

Product NDC: 42192-125
Labeler Name: Acella Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100818

Package Information of BPO 6 Foaming

Package NDC: 42192-125-60
Package Description: 60 PACKET in 1 CARTON (42192-125-60) > 3.2 g in 1 PACKET

NDC Information of BPO 6 Foaming

NDC Code 42192-125-60
Proprietary Name BPO 6 Foaming
Package Description 60 PACKET in 1 CARTON (42192-125-60) > 3.2 g in 1 PACKET
Product NDC 42192-125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BENZOYL PEROXIDE
Dosage Form Name CLOTH
Route Name TOPICAL
Start Marketing Date 20100818
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Acella Pharmaceuticals, LLC
Substance Name BENZOYL PEROXIDE
Strength Number 3.2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of BPO 6 Foaming


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