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ULTRA SEAL Triple Antibiotic - 42213-360-28 - (neomycin, polymixin, bacitracin)

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Drug Information of ULTRA SEAL Triple Antibiotic

Product NDC: 42213-360
Proprietary Name: ULTRA SEAL Triple Antibiotic
Non Proprietary Name: neomycin, polymixin, bacitracin
Active Ingredient(s): 400; 5; 5000    [iU]/g; mg/g; [iU]/g & nbsp;   neomycin, polymixin, bacitracin
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of ULTRA SEAL Triple Antibiotic

Product NDC: 42213-360
Labeler Name: Ultra Seal Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333B
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110412

Package Information of ULTRA SEAL Triple Antibiotic

Package NDC: 42213-360-28
Package Description: 1 TUBE in 1 CARTON (42213-360-28) > 28 g in 1 TUBE

NDC Information of ULTRA SEAL Triple Antibiotic

NDC Code 42213-360-28
Proprietary Name ULTRA SEAL Triple Antibiotic
Package Description 1 TUBE in 1 CARTON (42213-360-28) > 28 g in 1 TUBE
Product NDC 42213-360
Product Type Name HUMAN OTC DRUG
Non Proprietary Name neomycin, polymixin, bacitracin
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20110412
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Ultra Seal Corporation
Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 400; 5; 5000
Strength Unit [iU]/g; mg/g; [iU]/g
Pharmaceutical Classes

Complete Information of ULTRA SEAL Triple Antibiotic


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