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Genuine Triple Antibiotic - 52124-0003-3 - (BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE)

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Drug Information of Genuine Triple Antibiotic

Product NDC: 52124-0003
Proprietary Name: Genuine Triple Antibiotic
Non Proprietary Name: BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE
Active Ingredient(s): 400; 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 Genuine Triple Antibiotic

Product NDC: 52124-0003
Labeler Name: Genuine First Aid LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100216

Package Information of Genuine Triple Antibiotic

Package NDC: 52124-0003-3
Package Description: 100 PACKET in 1 CARTON (52124-0003-3) > .5 g in 1 PACKET

NDC Information of Genuine Triple Antibiotic

NDC Code 52124-0003-3
Proprietary Name Genuine Triple Antibiotic
Package Description 100 PACKET in 1 CARTON (52124-0003-3) > .5 g in 1 PACKET
Product NDC 52124-0003
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 20100216
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Genuine First Aid LLC
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 5; 5000
Strength Unit [iU]/g; mg/g; [iU]/g
Pharmaceutical Classes

Complete Information of Genuine Triple Antibiotic


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