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NON ALCOHOL HAND SANITIZER - 50260-500-09 - (Benzalkonium Chloride)

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Drug Information of NON ALCOHOL HAND SANITIZER

Product NDC: 50260-500
Proprietary Name: NON ALCOHOL HAND SANITIZER
Non Proprietary Name: Benzalkonium Chloride
Active Ingredient(s): .1    mL/100mL & nbsp;   Benzalkonium Chloride
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of NON ALCOHOL HAND SANITIZER

Product NDC: 50260-500
Labeler Name: Fercy Personal Care Products Co Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20101113

Package Information of NON ALCOHOL HAND SANITIZER

Package NDC: 50260-500-09
Package Description: 50 mL in 1 BOTTLE, PLASTIC (50260-500-09)

NDC Information of NON ALCOHOL HAND SANITIZER

NDC Code 50260-500-09
Proprietary Name NON ALCOHOL HAND SANITIZER
Package Description 50 mL in 1 BOTTLE, PLASTIC (50260-500-09)
Product NDC 50260-500
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium Chloride
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20101113
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Fercy Personal Care Products Co Limited
Substance Name BENZALKONIUM CHLORIDE
Strength Number .1
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of NON ALCOHOL HAND SANITIZER


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