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Antibiotic and Pain Relief - 59779-823-34 - (bacitracin zinc neomycin sulfate polymyxin b sulfate pramoxine hcl)

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Drug Information of Antibiotic and Pain Relief

Product NDC: 59779-823
Proprietary Name: Antibiotic and Pain Relief
Non Proprietary Name: bacitracin zinc neomycin sulfate polymyxin b sulfate pramoxine hcl
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 pramoxine hcl
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Antibiotic and Pain Relief

Product NDC: 59779-823
Labeler Name: CVS
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050103

Package Information of Antibiotic and Pain Relief

Package NDC: 59779-823-34
Package Description: 1 TUBE in 1 CARTON (59779-823-34) > 14 g in 1 TUBE

NDC Information of Antibiotic and Pain Relief

NDC Code 59779-823-34
Proprietary Name Antibiotic and Pain Relief
Package Description 1 TUBE in 1 CARTON (59779-823-34) > 14 g in 1 TUBE
Product NDC 59779-823
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacitracin zinc neomycin sulfate polymyxin b sulfate pramoxine hcl
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20050103
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name CVS
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 Antibiotic and Pain Relief


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