ALL-IN-ONE - 42853-102-13 - (BENZOYL PEROXIDE)

Alphabetical Index


Drug Information of ALL-IN-ONE

Product NDC: 42853-102
Proprietary Name: ALL-IN-ONE
Non Proprietary Name: BENZOYL PEROXIDE
Active Ingredient(s): 5.5    g/100mL & nbsp;   BENZOYL PEROXIDE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of ALL-IN-ONE

Product NDC: 42853-102
Labeler Name: AUGUSTUS BIOMED LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120225

Package Information of ALL-IN-ONE

Package NDC: 42853-102-13
Package Description: 100 mL in 1 TUBE (42853-102-13)

NDC Information of ALL-IN-ONE

NDC Code 42853-102-13
Proprietary Name ALL-IN-ONE
Package Description 100 mL in 1 TUBE (42853-102-13)
Product NDC 42853-102
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZOYL PEROXIDE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120225
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AUGUSTUS BIOMED LLC
Substance Name BENZOYL PEROXIDE
Strength Number 5.5
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of ALL-IN-ONE


General Information