Active Ingredient
Ethyl Alcohol 70.0%
Natural Hand Sanitizer
FDA Label NDC 79317-500
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kinh Buluc, S.a.p.i. De C.v. for the product Natural Hand Sanitizer (NDC 79317-500). 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, uses, warnings, do not use, stop use and ask a doctor if, 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
Uses
for handwashing to reduce bacteria on the skin that may cause disease. Recommended for repeated use.
Warnings
For external use only.
Flammable, keep away from heat and flame.
Do Not Use
in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
irritation and redness develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed, get medical assistance or contact a Poison Control Center right away.
Directions
Wet hands throroughly with product briskly rub hands together until dry. Supervise children under 6 years in the use of this product.
Other Information
Store at 10°C to 30°C (50°F to 86°F)
Avoid freezing or excessive heat above 40°C (104°F)
Inactive Ingredients
water, carboxypoliethylene, glycerin, aloe vera, thriethanolamine, EDTA
Package Labeling:
Bottle2 (Bottle2)
* Please review the disclaimer below.
