Antiseptic - 47682-214-33 - (benzalkonium chloride)

Alphabetical Index


Drug Information of Antiseptic

Product NDC: 47682-214
Proprietary Name: Antiseptic
Non Proprietary Name: benzalkonium chloride
Active Ingredient(s): 1.3    mg/mL & nbsp;   benzalkonium chloride
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Antiseptic

Product NDC: 47682-214
Labeler Name: Unifirst First Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120222

Package Information of Antiseptic

Package NDC: 47682-214-33
Package Description: 100 PACKET in 1 BOX (47682-214-33) > 2.5 mL in 1 PACKET (47682-214-99)

NDC Information of Antiseptic

NDC Code 47682-214-33
Proprietary Name Antiseptic
Package Description 100 PACKET in 1 BOX (47682-214-33) > 2.5 mL in 1 PACKET (47682-214-99)
Product NDC 47682-214
Product Type Name HUMAN OTC DRUG
Non Proprietary Name benzalkonium chloride
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120222
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Unifirst First Aid Corporation
Substance Name BENZALKONIUM CHLORIDE
Strength Number 1.3
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Antiseptic


General Information