sunmark - 49348-029-72 - (polymyxin B sulfate, bacitracin zinc, and neomycin sulfate)

Alphabetical Index


Drug Information of sunmark

Product NDC: 49348-029
Proprietary Name: sunmark
Non Proprietary Name: polymyxin B sulfate, bacitracin zinc, and neomycin sulfate
Active Ingredient(s): 400; 3.5; 5000    [iU]/g; mg/g; [iU]/g & nbsp;   polymyxin B sulfate, bacitracin zinc, and neomycin sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark

Product NDC: 49348-029
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19951214

Package Information of sunmark

Package NDC: 49348-029-72
Package Description: 1 TUBE in 1 CARTON (49348-029-72) > 28.4 g in 1 TUBE

NDC Information of sunmark

NDC Code 49348-029-72
Proprietary Name sunmark
Package Description 1 TUBE in 1 CARTON (49348-029-72) > 28.4 g in 1 TUBE
Product NDC 49348-029
Product Type Name HUMAN OTC DRUG
Non Proprietary Name polymyxin B sulfate, bacitracin zinc, and neomycin sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19951214
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 3.5; 5000
Strength Unit [iU]/g; mg/g; [iU]/g
Pharmaceutical Classes

Complete Information of sunmark


General Information