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Triple Antibiotic - 61010-5600-2 - (bacitracin zinc, neomycin sulfate, polymyxin b sulfate)

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Drug Information of Triple Antibiotic

Product NDC: 61010-5600
Proprietary Name: Triple Antibiotic
Non Proprietary Name: bacitracin zinc, neomycin sulfate, polymyxin b sulfate
Active Ingredient(s): 400; 3.5; 5000    [USP'U]/g; mg/g; [USP'U]/g & nbsp;   bacitracin zinc, neomycin sulfate, polymyxin b sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 61010-5600
Labeler Name: Safetec of America, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110808

Package Information of Triple Antibiotic

Package NDC: 61010-5600-2
Package Description: 144 POUCH in 1 BOX (61010-5600-2) > .9 g in 1 POUCH (61010-5600-1)

NDC Information of Triple Antibiotic

NDC Code 61010-5600-2
Proprietary Name Triple Antibiotic
Package Description 144 POUCH in 1 BOX (61010-5600-2) > .9 g in 1 POUCH (61010-5600-1)
Product NDC 61010-5600
Product Type Name HUMAN OTC DRUG
Non Proprietary Name bacitracin zinc, neomycin sulfate, polymyxin b sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20110808
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Safetec of America, Inc.
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 3.5; 5000
Strength Unit [USP'U]/g; mg/g; [USP'U]/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


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