Organic choice hand sanitizer

Manufacturer
TAHITI AU PTY LTD
Effective date
2020-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:18

Label at a glance#

ProductOrganic choice hand sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Apply Organic Choice hand sanitiser evenly onto palm of hand. Rub hands together for 20 seconds and allow air dry without wiping. Do not use on broken or inflamed skin.

Storage and handling

Store below 30°C keep out of direct sunlight.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

EthonaI 75% V/v

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on skin.
Recomm ended for repeated use.

Warnings

WARNINGS SECTION

For external use only.
Flammable. Keep away from sources of fire or flame.

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age On open skin wounds

OTC - WHEN USING SECTION

Keep away from eyes, in case of contact, rines eyes with water.

OTC - STOP USE SECTION

Redness or irritation develops and issues persist seek Medical attention.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, contact a doctor or Poisons Information Centre.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply Organic Choice hand sanitiser evenly onto palm of hand.
Rub hands together for 20 seconds and allow air dry without wiping.
Do not use on broken or inflamed skin.

Other information

STORAGE AND HANDLING SECTION

Store below 30°C
keep out of direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Aloe Vera, Eucalyptus Leaf Oil, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate , Crosspolymer, Triethanolamine, Vitamin E , Vegetable Glycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

001001

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79746-001-01Organic choice hand sanitizer50 mL in 1 BOTTLEGEL501
79746-001-02Organic choice hand sanitizer100 mL in 1 BOTTLEGEL1001
79746-001-03Organic choice hand sanitizer236 mL in 1 BOTTLEGEL2361
79746-001-04Organic choice hand sanitizer250 mL in 1 BOTTLEGEL2501
79746-001-05Organic choice hand sanitizer355 mL in 1 BOTTLEGEL3551
79746-001-06Organic choice hand sanitizer500 mL in 1 BOTTLEGEL5001
79746-001-07Organic choice hand sanitizer1000 mL in 1 BOTTLEGEL10001
79746-001-08Organic choice hand sanitizer1500 mL in 1 BOTTLEGEL15001
79746-001-09Organic choice hand sanitizer3780 mL in 1 BOTTLEGEL37801
79746-001-10Organic choice hand sanitizer5000 mL in 1 BOTTLEGEL50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79746-001ORGANIC CHOICE HAND SANITIZER GEL [TAHITI AU PTY LTD]1Legacy NDC, 10 package rows20200723_ab03807a-d319-7774-e053-2a95a90ae539.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
ab03807a-d30b-7774-e053-2a95a90ae539ab03807a-d319-7774-e053-2a95a90ae5392020-07-22WarningsExact identifier
spl id: ab03807a-d30b-7774-e053-2a95a90ae539
spl set id: ab03807a-d319-7774-e053-2a95a90ae539

Reported adverse events (FAERS/openFDA)#

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