Active Ingredient(S)
Ethyl Alcohol 62% v/v. Purpose: Antiseptic
Hand Sanitizer-gel
FDA Label NDC 50663-003
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 Hand Sanitizer-gel (NDC 50663-003). 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, warnings, otc - when using, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from fire or flame
Otc - When Using
When using this product keep 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.
Otc - Keep Out Of Reach Of Children
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 Propane! • lsopropyl Myrlstate • T-Butyl Alcohol
Questions
? 1-877-777-3277
Legal Entity
®,TM,©2018 Distributed by
Henkel Corporation,
Rocky Hill, CT 06067
www.dialprofessional.com
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