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Triple Antibiotic - 50607-5600-2 - (Triple Antibiotic)

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Drug Information of Triple Antibiotic

Product NDC: 50607-5600
Proprietary Name: Triple Antibiotic
Non Proprietary Name: Triple Antibiotic
Active Ingredient(s): 400; 5; 5000    1/g; mg/g; 1/g & nbsp;   Triple Antibiotic
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic

Product NDC: 50607-5600
Labeler Name: B8 Sales, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100501

Package Information of Triple Antibiotic

Package NDC: 50607-5600-2
Package Description: 144 POUCH in 1 BOX (50607-5600-2) > .9 g in 1 POUCH

NDC Information of Triple Antibiotic

NDC Code 50607-5600-2
Proprietary Name Triple Antibiotic
Package Description 144 POUCH in 1 BOX (50607-5600-2) > .9 g in 1 POUCH
Product NDC 50607-5600
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Triple Antibiotic
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20100501
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name B8 Sales, Inc.
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 5; 5000
Strength Unit 1/g; mg/g; 1/g
Pharmaceutical Classes

Complete Information of Triple Antibiotic


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