Active Ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 50049-123
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 50049-123). 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
Uses Hand sanitizer to decrease bacteria on the skin.
Warnings
Warnings For external use only - hands
Flammable. Keep away from heat or flame.
When using this product
Avoid contact with eyes. In case of contact flush eyes thoroughly with
water.
Stop and ask doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children If swallowed, get medical help or
contact Poison Control Center right away.
Directions
Wet hands thoroughly with product and allow to dry
without wiping. Children under 6 years of age should be supervised
when using this product.
Inactive Ingredients
Water (Aqua), Glycerin, Butylene Glycol,
Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Fragrance
* Please review the disclaimer below.
