Active Ingredient(S)
EthonaI 75% V/v
Organic Choice Hand Sanitizer
FDA Label NDC 79746-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tahiti Au Pty Ltd for the product Organic Choice Hand Sanitizer (NDC 79746-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
To decrease bacteria on skin.
Recomm ended for repeated use.
Warnings
For external use only.
Flammable. Keep away from sources of fire or flame.
Do Not Use
In children less than 2 months of age On open skin wounds
Otc - When Using
Keep away from eyes, in case of contact, rines eyes with water.
Otc - Stop Use
Redness or irritation develops and issues persist seek Medical attention.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, contact a doctor or Poisons Information Centre.
Directions
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
Store below 30°C
keep out of direct sunlight.
Inactive Ingredients
Aqua, Aloe Vera, Eucalyptus Leaf Oil, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate , Crosspolymer, Triethanolamine, Vitamin E , Vegetable Glycerin
Package Label - Principal Display Panel
001 (001)
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