Home > National Drug Code (NDC) > Triple Antibiotic Ointment

Triple Antibiotic Ointment - 0713-0268-31 - (Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate)

Alphabetical Index


Drug Information of Triple Antibiotic Ointment

Product NDC: 0713-0268
Proprietary Name: Triple Antibiotic Ointment
Non Proprietary Name: Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate
Active Ingredient(s): 400; 3.5; 5000    [USP'U]/g; mg/g; [USP'U]/g & nbsp;   Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Triple Antibiotic Ointment

Product NDC: 0713-0268
Labeler Name: G&W Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19950111

Package Information of Triple Antibiotic Ointment

Package NDC: 0713-0268-31
Package Description: 28.4 g in 1 TUBE (0713-0268-31)

NDC Information of Triple Antibiotic Ointment

NDC Code 0713-0268-31
Proprietary Name Triple Antibiotic Ointment
Package Description 28.4 g in 1 TUBE (0713-0268-31)
Product NDC 0713-0268
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Polymyxin B Sulfate, Bacitracin Zinc, Neomycin Sulfate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19950111
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name G&W Laboratories, Inc.
Substance Name BACITRACIN ZINC; NEOMYCIN; 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 Ointment


General Information