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Antibiotic and Pain Relief - 59779-822-56 - (Neomycin Sulfate, Polymyxin B Sulfate, Pramoxine HCI)

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Drug Information of Antibiotic and Pain Relief

Product NDC: 59779-822
Proprietary Name: Antibiotic and Pain Relief
Non Proprietary Name: Neomycin Sulfate, Polymyxin B Sulfate, Pramoxine HCI
Active Ingredient(s): 3.5; 10000; 10    mg/g; [iU]/g; mg/g & nbsp;   Neomycin Sulfate, Polymyxin B Sulfate, Pramoxine HCI
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Antibiotic and Pain Relief

Product NDC: 59779-822
Labeler Name: Consumer Value Stores
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110101

Package Information of Antibiotic and Pain Relief

Package NDC: 59779-822-56
Package Description: 1 TUBE in 1 CARTON (59779-822-56) > 28 g in 1 TUBE

NDC Information of Antibiotic and Pain Relief

NDC Code 59779-822-56
Proprietary Name Antibiotic and Pain Relief
Package Description 1 TUBE in 1 CARTON (59779-822-56) > 28 g in 1 TUBE
Product NDC 59779-822
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Neomycin Sulfate, Polymyxin B Sulfate, Pramoxine HCI
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Consumer Value Stores
Substance Name NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Strength Number 3.5; 10000; 10
Strength Unit mg/g; [iU]/g; mg/g
Pharmaceutical Classes

Complete Information of Antibiotic and Pain Relief


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