Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 50049-010
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 50049-010). 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 Hand Sanitizing
Warnings
■For extemal use only
■Flammable. Keep away from fire or flame
When using this product
■Keep out of eyes. In case of contact with eyes, flush thoroughly with water
1 Avoid contact with open skin
■Do not inhale or ingest
Stop use and ask a doctor
■If skin irritation or redness develops
Otc - Keep Out Of Reach Of Children
■Keep out of reach of children. Children under 6 years of age use only under adult supervision
Directions
Wet hands thoroughly with product and allow to dry without wiping
Not recommended for infants
Inactive Ingredients
Alcohol, Water (Aqua), Glycerin, Butylene Glyool, Carbomer, Aminomethyl
Propanol, Aloe Barbadensis Leaf Extract.
Package Label.Principal Display Panel
1 (010)
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