Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 73788-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Huiji Biotechnology Co., Ltd. for the product Hand Sanitizer (NDC 73788-102). 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, purpose, use, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For Hand Sanitizing
Flammable. Keep away from fire or fiame
Warnings
Keep out of eyes. In case of contact with eyes,
flush thoroughly with water
Avoid contact with open skin
Do not inhale or ingest
Stop use and ask a doctor
If skin iritation or redness develops
Otc - Keep Out Of Reach Of Children
keep out of reach of children
if swallowed, get medical help or contact a Poison Control Center right away.
Directions
Directions■Wet hands thoroughly with
product and allow to dry without wiping 1 Children
under 6 years of age use only under adult
supervision■Not recommended for infants
Other Information
1 Do not store above 105°F
1 May discolor some fabrics
Inactive Ingredients
Water, Glycerin, Aloe Barbadensis Leaf extract, Carbomer, Tocopheryl
Acetate, Triethanolamine
* Please review the disclaimer below.
