Active Ingredient(S)
Ethyl Alcohol 62% v/v.
Henkel Beauty Care Professional
FDA Label NDC 50663-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zotos International Inc for the product Henkel Beauty Care Professional (NDC 50663-005). 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, uses, warnings, when using this product, 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
Hand Sanitizer to help reduce bacteria.
*Encountered in away-from-home settings.
Warnings
For external use only.
Flammable. Keep away from fire or flame
When Using This Product
avoid contact with face, eyes, and broken skin. if eye contact occurs, flush thoroughly with water and seek medical advice.
Stop Use And Ask A Doctor If
irritation or redness develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wet hands thoroughly with product and rub into skin until dry.
Children under 6 years of age should be supervised by an adult when using this product.
Inactive Ingredients
Aqua (Water, Eau)• Propylene Glycol• Glycerin• Carbomer • Aminomethyl Propanol • lsopropyl Myristate • T-Butyl Alcohol
Questions?
1-800-258-3425
Legal Entity
Distributed by Henkel Corporation, Culver City, CA 90230
Made in USA of globally sourced ingredients/components.
* Please review the disclaimer below.
