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Neosporin Plus Pain Relief - 58232-9612-1 - (Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride)

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Drug Information of Neosporin Plus Pain Relief

Product NDC: 58232-9612
Proprietary Name: Neosporin Plus Pain Relief
Non Proprietary Name: Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride
Active Ingredient(s): 500; 3.5; 10000; 10    [iU]/g; mg/g; [iU]/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 Neosporin Plus Pain Relief

Product NDC: 58232-9612
Labeler Name: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110201

Package Information of Neosporin Plus Pain Relief

Package NDC: 58232-9612-1
Package Description: 1 BOTTLE, PUMP in 1 BLISTER PACK (58232-9612-1) > 3.7 g in 1 BOTTLE, PUMP

NDC Information of Neosporin Plus Pain Relief

NDC Code 58232-9612-1
Proprietary Name Neosporin Plus Pain Relief
Package Description 1 BOTTLE, PUMP in 1 BLISTER PACK (58232-9612-1) > 3.7 g in 1 BOTTLE, PUMP
Product NDC 58232-9612
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 20110201
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Strength Number 500; 3.5; 10000; 10
Strength Unit [iU]/g; mg/g; [iU]/g; mg/g
Pharmaceutical Classes

Complete Information of Neosporin Plus Pain Relief


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