Label: ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER- benzalkonium chloride liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 76452-001-00 - Packager: SAS Healthcare Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 26, 2011
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses:
- Warnings:
- Directions:
- Inactive Ingredients:
- Manufactured for:
- Zaliex ALCOHOL-FREE Antiseptic Foam Hand Sanitizer 50ml
-
INGREDIENTS AND APPEARANCE
ZALIEX ALCOHOL-FREE ANTISEPTIC HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76452-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) GLYCERETH-2 COCOATE (UNII: JWM00VS7HC) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76452-001-00 50 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/26/2011 Labeler - SAS Healthcare Inc (248055696) Establishment Name Address ID/FEI Business Operations Artemis Bio-Solutions Inc. 963442541 manufacture