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Ear Wax Remover - 0904-6004-35 - (CARBAMIDE PEROXIDE)

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Drug Information of Ear Wax Remover

Product NDC: 0904-6004
Proprietary Name: Ear Wax Remover
Non Proprietary Name: CARBAMIDE PEROXIDE
Active Ingredient(s): 65    mg/mL & nbsp;   CARBAMIDE PEROXIDE
Administration Route(s): AURICULAR (OTIC)
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Ear Wax Remover

Product NDC: 0904-6004
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN OTC DRUG
FDA Application Number: part344
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090527

Package Information of Ear Wax Remover

Package NDC: 0904-6004-35
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON (0904-6004-35) > 15 mL in 1 BOTTLE, DISPENSING

NDC Information of Ear Wax Remover

NDC Code 0904-6004-35
Proprietary Name Ear Wax Remover
Package Description 1 BOTTLE, DISPENSING in 1 CARTON (0904-6004-35) > 15 mL in 1 BOTTLE, DISPENSING
Product NDC 0904-6004
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CARBAMIDE PEROXIDE
Dosage Form Name LIQUID
Route Name AURICULAR (OTIC)
Start Marketing Date 20090527
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Major Pharmaceuticals
Substance Name CARBAMIDE PEROXIDE
Strength Number 65
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Ear Wax Remover


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