Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer Gel
FDA Label NDC 73788-101
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 Gel (NDC 73788-101). 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 to reduce bacteria
on the skin.
Warnings
Flammable. Keep away from fire or
flame. For external use only. Keep
out of reach of children. Keep away
from eyes. Do not inhale or ingest.
Stop use and ask doctor if irritation
or redness develops.
Keep Out Of Reach Of Children
â– Keep out of reach of children
Directions
Squeeze small amount in your
palm and briskly rub hands
together, and allow to air dry.
For children under 6, use with adult
supervision. Not recommended for
infants.
Other Information
Store below 110 F (43 C). May
discolor certain fabrics or surfaces
Inactive Ingredients
Inactive ingredients Water,
Glycerin, Aloe barbadensis leaf extract,
Carbomer.Tocopheryl Acetate,
Triethanolamine
Package Label.Principal Display Panel
11 (0501label11)
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