Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 73788-100
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 73788-100). 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, 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
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
Keep Out Of Reach Of Children
■Keep out of reach of children. Children under 6
years of age use only under adult supervision
■Not recommended for infants
Directions
Wet hands thoroughly with product and allow to dry without wiping
Other Information
1 Do not store above 105°F
1 May discolor some fabrics
Inactive Ingredients
Alcohol, Water (Aqua), Glycerin, Butylene Glycol, Carbomer,
Aminomethyl Propanol, Aloe Barbadensis Leaf Extract
Package Label.Principal Display Panel
1 (73788100)
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