FDA.reportPublic FDA data

Zaliex Alcohol-Free Foaming Hand Sanitizer

Manufacturer
SAS Healthcare Inc | Artemis Bio-Solutions Inc.
Effective date
2012-09-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:33:01

Label at a glance#

ProductZaliex Alcohol-Free Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing, to eliminate harmful bacteria and germs on skin. Use as part of your daily cleansing routine. Recommended for repeated use.

Dosage and administration

Pump a small amount of foam into palm of hand Run thoroughly over all surfaces of both hands Rub hands together briskly until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

For hand sanitizing, to eliminate harmful bacteria and germs on skin.
Use as part of your daily cleansing routine.
Recommended for repeated use.

Warnings:

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops, or if condition persists.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Pump a small amount of foam into palm of hand
  • Run thoroughly over all surfaces of both hands
  • Rub hands together briskly until dry

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Manufactured for:

SPL UNCLASSIFIED SECTION

Zaliex

Suite 210, 4 Robert Speck Parkway,

Mississauga, Ontario, L4Z1S1, Canada

Zaliex Alcohol-Free Foaming Hand Sanitizer 1L (76452-004-00)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZaliexHandSanitizer1000mLFrench
ZaliexHandSanitizer1000mLFrench


DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN2
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD2
1038799benzalkonium chloride 0.1 % Topical FoamSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130793573137722GTIN-13: 0793573137722
EAN-13: 0793573137722
GTIN-12: 793573137722
UPC-A: 793573137722
GTIN storage (14 digits): 00793573137722		ZaliexHandSanitizer1000mLFrench.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76452-004-002020-01-31C16284748780-19d75b9d0-2ebd-f424-e053-dadaa90a57ceZaliex Alcohol-Free Foaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76452-004-00Zaliex Alcohol-Free Foaming Hand Sanitizer1 L in 1 BOTTLELIQUID12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76452-004ZALIEX ALCOHOL-FREE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [SAS HEALTHCARE INC]2Legacy NDC, 1 package rows20120912_2e80a8ba-9fa9-44b9-849b-ae590d761a2e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
BENZALKONIUM CHLORIDEACTIVE INGREDIENTF5UM2KM3W72
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y2
BEHENTRIMONIUM CHLORIDEINACTIVE INGREDIENTX7GNG3S47T2
DIHYDROXYETHYL COCAMINE OXIDEINACTIVE INGREDIENT8AR51R3BL52
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDEINACTIVE INGREDIENT0Y0NQR2GH12
GLYCERETH-2 COCOATEINACTIVE INGREDIENTJWM00VS7HC2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76452-00476452-004-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE0Y0NQR2GH1IACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
BEHENTRIMONIUM CHLORIDEX7GNG3S47TIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2b543a16-e2bf-4b00-822e-01326f57cd0e2e80a8ba-9fa9-44b9-849b-ae590d761a2e2012-09-12WarningsExact identifier
spl id: 2b543a16-e2bf-4b00-822e-01326f57cd0e
spl set id: 2e80a8ba-9fa9-44b9-849b-ae590d761a2e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.