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TRIPLE ANTIBIOTIC - 0904-0734-36 - (bacitracin zinc neomycin sulfate polymyxin b sulfate)

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Drug Information of TRIPLE ANTIBIOTIC

Product NDC: 0904-0734
Proprietary Name: TRIPLE ANTIBIOTIC
Non Proprietary Name: bacitracin zinc neomycin sulfate polymyxin b sulfate
Active Ingredient(s): 400; 3.5; 5000    [iU]/g; mg/g; [iU]/g & nbsp;   bacitracin zinc neomycin sulfate polymyxin b sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of TRIPLE ANTIBIOTIC

Product NDC: 0904-0734
Labeler Name: Major
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110601

Package Information of TRIPLE ANTIBIOTIC

Package NDC: 0904-0734-36
Package Description: 14 g in 1 TUBE (0904-0734-36)

NDC Information of TRIPLE ANTIBIOTIC

NDC Code 0904-0734-36
Proprietary Name TRIPLE ANTIBIOTIC
Package Description 14 g in 1 TUBE (0904-0734-36)
Product NDC 0904-0734
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacitracin zinc neomycin sulfate polymyxin b sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20110601
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Major
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 TRIPLE ANTIBIOTIC


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