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Triple Antibiotic - 54473-578-01 - (Bacitracin zinc and Neomycin and Polymyxin B sulfate)

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Drug Information of Triple Antibiotic

Product NDC: 54473-578
Proprietary Name: Triple Antibiotic
Non Proprietary Name: Bacitracin zinc and Neomycin and Polymyxin B sulfate
Active Ingredient(s): 500; 3.5; 10000    [iU]/g; mg/g; [iU]/g & nbsp;   Bacitracin zinc and Neomycin and Polymyxin B sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 54473-578
Labeler Name: Melaleuca, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19950701

Package Information of Triple Antibiotic

Package NDC: 54473-578-01
Package Description: 14 g in 1 TUBE (54473-578-01)

NDC Information of Triple Antibiotic

NDC Code 54473-578-01
Proprietary Name Triple Antibiotic
Package Description 14 g in 1 TUBE (54473-578-01)
Product NDC 54473-578
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin zinc and Neomycin and Polymyxin B sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19950701
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Melaleuca, Inc.
Substance Name BACITRACIN ZINC; NEOMYCIN; POLYMYXIN B SULFATE
Strength Number 500; 3.5; 10000
Strength Unit [iU]/g; mg/g; [iU]/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


General Information