Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 73788-104
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 73788-104). 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 handwashing to decrease bacteria on
the skin.
Warnings
Flammable. Keep away from fire or flame.
Do not use
●in children less than 2 months of age
●on open skin wounds
For external use only
When using this product avoid contact with eyes.
If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash
develops and continues for more than 72 hours.
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
●Take a palmful (5grams) of product in one hand.
●Spread on both hands and rub into skin
until dry (approximately 1 to 2 minutes).
●Supervise children under 6 years of age when
using this product to avoid swallowing.
Other Information
1 Do not store above 105°F
1 May discolor some fabrics
Inactive Ingredients
Carbomer, Fragrance, Glycerin, Triethanolamine,
Water,
* Please review the disclaimer below.
