Active Ingredient[S]
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 74242-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kem Krest Llc for the product Hand Sanitizer (NDC 74242-110). 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[s], purpose, use[s], warnings, otc - when using, otc - stop use, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use[S]
For hand washing to decrease bacteria on the skin. Recommended for repeated use.
Warnings
Flammable. Keep away from fire or flame. For external use only. Avoid contact with broken skin.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
If swallowed get medical help.
Directions
Not recommended for infants. Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.
Other Information
Do not store above 110 F (43°C). May discolor some fabrics.
Inactive Ingredients
Water(Aqua), Glycerin, propylene Glycol, Acrylates/C10-30Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, fragrance(Parfum), Denatonium Benzoate, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Maltodextrin.
Package Label.Principal Display Panel
Image Of Bottle Label (10oz)
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