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Triple Antibiotic Plus Pain Relief - 59970-040-01 - (Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride)

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Drug Information of Triple Antibiotic Plus Pain Relief

Product NDC: 59970-040
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: 59970-040
Labeler Name: Navarro Discount Pharmacies,LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120801

Package Information of Triple Antibiotic Plus Pain Relief

Package NDC: 59970-040-01
Package Description: 1 TUBE in 1 CARTON (59970-040-01) > 28.3 g in 1 TUBE

NDC Information of Triple Antibiotic Plus Pain Relief

NDC Code 59970-040-01
Proprietary Name Triple Antibiotic Plus Pain Relief
Package Description 1 TUBE in 1 CARTON (59970-040-01) > 28.3 g in 1 TUBE
Product NDC 59970-040
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 20120801
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Navarro Discount Pharmacies,LLC
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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