Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 77753-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shandishi Biological Technology Co., Ltd. for the product Hand Sanitizer (NDC 77753-003). 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, 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
For handwashing to decrease bacteria on the skin.
Warnings
Flammable, Keep away fromn fire or flame.
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 skin iritation 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
●Place enough product in your palm to thoroughly cover
your hands.●Children under 6 years of age should be
supervised when using this product.●Rub hands together
briskly until dry.●Not recommended for infants.
Inactive Ingredients
Aloe vera leaf juice, Glycerin, Fragrance(parfum) ,Water
* Please review the disclaimer below.
