sunmark - 49348-600-72 - (polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride)

Alphabetical Index


Drug Information of sunmark

Product NDC: 49348-600
Proprietary Name: sunmark
Non Proprietary Name: polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride
Active Ingredient(s): 500; 3.5; 10000; 10    [iU]/g; mg/g; [iU]/g; mg/g & nbsp;   polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark

Product NDC: 49348-600
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120331

Package Information of sunmark

Package NDC: 49348-600-72
Package Description: 1 TUBE in 1 CARTON (49348-600-72) > 28.4 g in 1 TUBE

NDC Information of sunmark

NDC Code 49348-600-72
Proprietary Name sunmark
Package Description 1 TUBE in 1 CARTON (49348-600-72) > 28.4 g in 1 TUBE
Product NDC 49348-600
Product Type Name HUMAN OTC DRUG
Non Proprietary Name polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120331
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Strength Number 500; 3.5; 10000; 10
Strength Unit [iU]/g; mg/g; [iU]/g; mg/g
Pharmaceutical Classes

Complete Information of sunmark


General Information