Handi-San - 62712-575-27 - (BENZETHONIUM CHLORIDE)

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Drug Information of Handi-San

Product NDC: 62712-575
Proprietary Name: Handi-San
Non Proprietary Name: BENZETHONIUM CHLORIDE
Active Ingredient(s): 2    mg/mL & nbsp;   BENZETHONIUM CHLORIDE
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Handi-San

Product NDC: 62712-575
Labeler Name: Atco International
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20060101

Package Information of Handi-San

Package NDC: 62712-575-27
Package Description: 800 mL in 1 CARTRIDGE (62712-575-27)

NDC Information of Handi-San

NDC Code 62712-575-27
Proprietary Name Handi-San
Package Description 800 mL in 1 CARTRIDGE (62712-575-27)
Product NDC 62712-575
Product Type Name HUMAN OTC DRUG
Non Proprietary Name BENZETHONIUM CHLORIDE
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20060101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Atco International
Substance Name BENZETHONIUM CHLORIDE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Handi-San


General Information