Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 73788-004
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 73788-004). 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
■ Hand sanitizer to help decrease bacteria on
the skin
■When water, soap & towel are not
available.
■Recommended for repeated use,
Warnings
For external use only■Highly inflammable
Keep away from heat, sparks, open flame, hot surfaces.
Do not apply around eyes. Do not use in ears & mouth.
Avoid contact with eyes
If in eyes: rinse well with clean water
Stop use and seek medical advice or attention if
irritation persists
Keep Out Of Reach Of Children
Keep out of reach of children. Children must be
supervised in use of this product
Directions
■Squeeze the bottle after removing the lid and thoroughly
spread on both hands. Rub into skin until dry
Other Information Avoid contact with fabrics as
could cause discolouration
Inactive Ingredients
Water, Glycerin, Aloe
barbadensis leaf extract, Carbomer.
Tocopheryl Acetate, Triethanolamine
* Please review the disclaimer below.
