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Benzalkonium Chloride - 53329-931-09 - (Benzalkonium Chloride)

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Drug Information of Benzalkonium Chloride

Product NDC: 53329-931
Proprietary Name: Benzalkonium Chloride
Non Proprietary Name: Benzalkonium Chloride
Active Ingredient(s): .04    mg/100mL & nbsp;   Benzalkonium Chloride
Administration Route(s): TOPICAL
Dosage Form(s): CLOTH
Coding System: National Drug Codes(NDC)

Labeler Information of Benzalkonium Chloride

Product NDC: 53329-931
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20070101

Package Information of Benzalkonium Chloride

Package NDC: 53329-931-09
Package Description: 100 PACKET in 1 BOX (53329-931-09) > 1 APPLICATOR in 1 PACKET > 5 mL in 1 APPLICATOR

NDC Information of Benzalkonium Chloride

NDC Code 53329-931-09
Proprietary Name Benzalkonium Chloride
Package Description 100 PACKET in 1 BOX (53329-931-09) > 1 APPLICATOR in 1 PACKET > 5 mL in 1 APPLICATOR
Product NDC 53329-931
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Benzalkonium Chloride
Dosage Form Name CLOTH
Route Name TOPICAL
Start Marketing Date 20070101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Medline Industries, Inc.
Substance Name BENZALKONIUM CHLORIDE
Strength Number .04
Strength Unit mg/100mL
Pharmaceutical Classes

Complete Information of Benzalkonium Chloride


General Information