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Triple Antibiotic - 62011-0098-1 - (Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate)

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Drug Information of Triple Antibiotic

Product NDC: 62011-0098
Proprietary Name: Triple Antibiotic
Non Proprietary Name: Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate
Active Ingredient(s): 400; 3.5; 5000    [USP'U]/g; mg/g; [USP'U]/g & nbsp;   Bacitracin Zinc, Neomycin Sulfate, 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: 62011-0098
Labeler Name: Health Mart
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120321

Package Information of Triple Antibiotic

Package NDC: 62011-0098-1
Package Description: 1 TUBE in 1 CARTON (62011-0098-1) > 28.4 g in 1 TUBE

NDC Information of Triple Antibiotic

NDC Code 62011-0098-1
Proprietary Name Triple Antibiotic
Package Description 1 TUBE in 1 CARTON (62011-0098-1) > 28.4 g in 1 TUBE
Product NDC 62011-0098
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120321
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Health Mart
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 3.5; 5000
Strength Unit [USP'U]/g; mg/g; [USP'U]/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


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