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Earwax Removal Kit - 62011-0169-1 - (Earwax Removal Kit)

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Drug Information of Earwax Removal Kit

Product NDC: 62011-0169
Proprietary Name: Earwax Removal Kit
Non Proprietary Name: Earwax Removal Kit
Active Ingredient(s): 6.5    mg/100mL & nbsp;   Earwax Removal Kit
Administration Route(s): AURICULAR (OTIC)
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Earwax Removal Kit

Product NDC: 62011-0169
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part344
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120206

Package Information of Earwax Removal Kit

Package NDC: 62011-0169-1
Package Description: 15 mL in 1 BOTTLE (62011-0169-1)

NDC Information of Earwax Removal Kit

NDC Code 62011-0169-1
Proprietary Name Earwax Removal Kit
Package Description 15 mL in 1 BOTTLE (62011-0169-1)
Product NDC 62011-0169
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Earwax Removal Kit
Dosage Form Name LIQUID
Route Name AURICULAR (OTIC)
Start Marketing Date 20120206
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name CARBAMIDE PEROXIDE
Strength Number 6.5
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of Earwax Removal Kit


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