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Triple Antibiotic Plus Pain Relief - 51672-2027-2 - (Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride)

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Drug Information of Triple Antibiotic Plus Pain Relief

Product NDC: 51672-2027
Proprietary Name: Triple Antibiotic Plus Pain Relief
Non Proprietary Name: Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride
Active Ingredient(s): 500; 3.5; 10000; 10    [USP'U]/g; mg/g; [USP'U]/g; mg/g & nbsp;   Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic Plus Pain Relief

Product NDC: 51672-2027
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120331

Package Information of Triple Antibiotic Plus Pain Relief

Package NDC: 51672-2027-2
Package Description: 1 TUBE in 1 CARTON (51672-2027-2) > 28.4 g in 1 TUBE

NDC Information of Triple Antibiotic Plus Pain Relief

NDC Code 51672-2027-2
Proprietary Name Triple Antibiotic Plus Pain Relief
Package Description 1 TUBE in 1 CARTON (51672-2027-2) > 28.4 g in 1 TUBE
Product NDC 51672-2027
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20120331
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Strength Number 500; 3.5; 10000; 10
Strength Unit [USP'U]/g; mg/g; [USP'U]/g; mg/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic Plus Pain Relief


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