FDA.reportPublic FDA data

HAND SANITIZER

Manufacturer
CANADA GREEN GATE KOZMETIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI
Effective date
2020-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:47

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other information: Do not store above 105°F

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses: Recommended for repeated use.

WARNINGS SECTION

Warnings: For external use only-hands.

When using this product: Keep out of eyes in case of contact with eyes. Flush thoroughly with water. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly with product and allow to dry without wiping. 

STORAGE AND HANDLING SECTION

Other information: Do not store above 105°F

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Glycerin, Carbomer, Triethanolamine

SPL UNCLASSIFIED SECTION

NEW

Kills 99.9% of germs WITHOUT WATER

Manufacturer:

CANADA GREEN GATE

Kozmetik Ürüneri San. ve Tic. A.S.

ADANA HACI SABACI ORG.SAN.BÖL.

OSB TOROSLAR CADDESI NO:17/1

SARIÇAM 7 ADANA / TURKEY 

PH: +90 322 394 48 50 FAX: 394 48 51

info@canadagreengate.com

www.canadagreengate.com

MADE IN TURKEY

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78726-100-102022-01-28C16284748780-1d6a99b39-c24f-a426-e053-dadaa90af4c2CLiNiCO HAND SANITIZER
78726-100-252022-01-28C16284748780-1d6a99b39-c24f-a426-e053-dadaa90af4c2CLiNiCO HAND SANITIZER
78726-100-502022-01-28C16284748780-1d6a99b39-c24f-a426-e053-dadaa90af4c2CLiNiCO HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78726-100-10HAND SANITIZER100 mL in 1 BOTTLE, PLASTICGEL1001
78726-100-25HAND SANITIZER250 mL in 1 BOTTLE, PLASTICGEL2501
78726-100-50HAND SANITIZER500 mL in 1 BOTTLE, PLASTICGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78726-100HAND SANITIZER (ALCOHOL) GEL [CANADA GREEN GATE KOZMETIK URUNLERI SANAYI VE TICARET ANONIM SIRKETI]1Legacy NDC, 3 package rows20200610_17fc550b-b39b-4afe-a037-0b5db8f0e2c0.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78726-10078726-100-10, 78726-100-25, 78726-100-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT

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
2610ddb1-ca76-47be-898c-e820e977ad9a17fc550b-b39b-4afe-a037-0b5db8f0e2c02020-06-05WarningsExact identifier
spl id: 2610ddb1-ca76-47be-898c-e820e977ad9a
spl set id: 17fc550b-b39b-4afe-a037-0b5db8f0e2c0

Reported adverse events (FAERS/openFDA)#

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