Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 50049-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quanzhou Besthope Household Products Co.,ltd. for the product Hand Sanitizer (NDC 50049-100). 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■ Flammable
Keep away from fire or flame
Do not apply around eyes. Do not use in ears & mouth.
When using this product. avoid contact with eyes.
In case of contact flush eyes with water
Stop use and ask a doctor it redness or irritation
develop and persist for more than 72 hours
Keep Out Of Reach Of Children
Keep out of reach of children. Children must be
supervised in use of this product
Directions
Pump as needed into your palms and thoroughly
spread on both hands. Rub into skin until dry
Other Information Store at 20C(88" to 77"F)
may discolor fabrices
Inactive Ingredients
Aloohol, Water(Aqua), Glycenin, Butylene Glycol, Carbomer,Aminomethyl Propanol, Aloe Barbadensis Leaf Extract
* Please review the disclaimer below.
