Kuri Hand Sanitizer
FDA Label NDC 79560-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kuri Enterprises for the product Kuri Hand Sanitizer (NDC 79560-001). 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 drug facts, active ingredient, purpose, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 70%
Purpose
Antiseptic
Use
For hand-washing to decrease bacteria on the skin, only when water is not available.
Warnings
-Flammable, Keep away from heat or flame
-For external use only.
When Using This Product
- Do not get into eyes
- If contact occurs, rinse eyes thoroughly with water
Stop Use And Ask A Doctor If
- Irritation and redness develop
Keep Out Of Reach Of Children
Directions
- Wet hands thoroughly with product and allow to dry without wiping
Inactive Ingredients
Water, glycerin, Acrylates/dimethicome copolymer, Methylchloroisothiazolinone, Methylisothiazolinone, Triethanolamine, Aloe Vera Extract
Package Labeling
Label (Label)
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