DEBROX - 0135-0091-70 - (carbamide peroxide)

Alphabetical Index


Drug Information of DEBROX

Product NDC: 0135-0091
Proprietary Name: DEBROX
Non Proprietary Name: carbamide peroxide
Active Ingredient(s): .065    mg/mL & nbsp;   carbamide peroxide
Administration Route(s): AURICULAR (OTIC)
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of DEBROX

Product NDC: 0135-0091
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part344
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20101108

Package Information of DEBROX

Package NDC: 0135-0091-70
Package Description: 10 VIAL in 1 CARTON (0135-0091-70) > .7 mL in 1 VIAL (0135-0091-62)

NDC Information of DEBROX

NDC Code 0135-0091-70
Proprietary Name DEBROX
Package Description 10 VIAL in 1 CARTON (0135-0091-70) > .7 mL in 1 VIAL (0135-0091-62)
Product NDC 0135-0091
Product Type Name HUMAN OTC DRUG
Non Proprietary Name carbamide peroxide
Dosage Form Name LIQUID
Route Name AURICULAR (OTIC)
Start Marketing Date 20101108
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name CARBAMIDE PEROXIDE
Strength Number .065
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of DEBROX


General Information