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Triple Antibiotic - 67510-0070-1 - (Bacitracin Zinc, Neomycin Sulfate, Polymyxin B)

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Drug Information of Triple Antibiotic

Product NDC: 67510-0070
Proprietary Name: Triple Antibiotic
Non Proprietary Name: Bacitracin Zinc, Neomycin Sulfate, Polymyxin B
Active Ingredient(s): 400; 3.5; 5000    [USP'U]/g; mg/g; [USP'U]/g & nbsp;   Bacitracin Zinc, Neomycin Sulfate, Polymyxin B
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 67510-0070
Labeler Name: Kareway Product, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110810

Package Information of Triple Antibiotic

Package NDC: 67510-0070-1
Package Description: 1 TUBE in 1 BOX (67510-0070-1) > 28 g in 1 TUBE

NDC Information of Triple Antibiotic

NDC Code 67510-0070-1
Proprietary Name Triple Antibiotic
Package Description 1 TUBE in 1 BOX (67510-0070-1) > 28 g in 1 TUBE
Product NDC 67510-0070
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin Zinc, Neomycin Sulfate, Polymyxin B
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20110810
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kareway Product, Inc.
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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