Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 73788-109
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 73788-109). 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, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Use whenever soap and water are not available
Warnings
Flammable.Keep away from open flame and sources of heat
Avoid contact with eyes and flush eyes with water if occurred
Keep out of reach of children
lf irritation develops discontinue use and contact a physician
May discolour certain fabrics
Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
Apply liberally to hands for externaluse only
Inactive Ingredients
Water, Glycerin,Carbomer , Triethanolamine, Aloe Barbadensisleaf extract,Tocopheryl acetate
Package Label.Principal Display Panel
1 (108)
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