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Triple Antibiotic - 53210-1004-0 - (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE)

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Drug Information of Triple Antibiotic

Product NDC: 53210-1004
Proprietary Name: Triple Antibiotic
Non Proprietary Name: BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE
Active Ingredient(s): 400; 3.5; 5000    U/g; mg/g; U/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: 53210-1004
Labeler Name: Morales Distributors Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120926

Package Information of Triple Antibiotic

Package NDC: 53210-1004-0
Package Description: 1 TUBE in 1 BOX (53210-1004-0) > 28 g in 1 TUBE

NDC Information of Triple Antibiotic

NDC Code 53210-1004-0
Proprietary Name Triple Antibiotic
Package Description 1 TUBE in 1 BOX (53210-1004-0) > 28 g in 1 TUBE
Product NDC 53210-1004
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 20120926
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Morales Distributors Inc.
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 3.5; 5000
Strength Unit U/g; mg/g; U/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


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