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up and up first aid antibiotic pain relieving - 11673-891-58 - (Neomycin, Polymyxin B, Pramoxine HCl)

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Drug Information of up and up first aid antibiotic pain relieving

Product NDC: 11673-891
Proprietary Name: up and up first aid antibiotic pain relieving
Non Proprietary Name: Neomycin, Polymyxin B, Pramoxine HCl
Active Ingredient(s): 3.5; 10000; 10    mg/g; [USP'U]/g; mg/g & nbsp;   Neomycin, Polymyxin B, Pramoxine HCl
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of up and up first aid antibiotic pain relieving

Product NDC: 11673-891
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20091117

Package Information of up and up first aid antibiotic pain relieving

Package NDC: 11673-891-58
Package Description: 1 TUBE in 1 CARTON (11673-891-58) > 14 g in 1 TUBE

NDC Information of up and up first aid antibiotic pain relieving

NDC Code 11673-891-58
Proprietary Name up and up first aid antibiotic pain relieving
Package Description 1 TUBE in 1 CARTON (11673-891-58) > 14 g in 1 TUBE
Product NDC 11673-891
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Neomycin, Polymyxin B, Pramoxine HCl
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20091117
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Target Corporation
Substance Name NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Strength Number 3.5; 10000; 10
Strength Unit mg/g; [USP'U]/g; mg/g
Pharmaceutical Classes

Complete Information of up and up first aid antibiotic pain relieving


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