OBLITERATE - 49520-101-51 - (BENZOYL PEROXIDE)

Alphabetical Index


Drug Information of OBLITERATE

Product NDC: 49520-101
Proprietary Name: OBLITERATE
Non Proprietary Name: BENZOYL PEROXIDE
Active Ingredient(s): 5    g/100mL & nbsp;   BENZOYL PEROXIDE
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of OBLITERATE

Product NDC: 49520-101
Labeler Name: mybody
Product Type: HUMAN OTC DRUG
FDA Application Number: part333D
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120424

Package Information of OBLITERATE

Package NDC: 49520-101-51
Package Description: 1 BOTTLE in 1 BOX (49520-101-51) > 15 mL in 1 BOTTLE (49520-101-11)

NDC Information of OBLITERATE

NDC Code 49520-101-51
Proprietary Name OBLITERATE
Package Description 1 BOTTLE in 1 BOX (49520-101-51) > 15 mL in 1 BOTTLE (49520-101-11)
Product NDC 49520-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZOYL PEROXIDE
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20120424
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name mybody
Substance Name BENZOYL PEROXIDE
Strength Number 5
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of OBLITERATE


General Information