Otc - Active Ingredient
Ethyl alcohol 62%
Hello Kitty Hand Sanitizer
FDA Label NDC 54340-256
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Dial Corporation, A Henkel Company for the product Hello Kitty Hand Sanitizer (NDC 54340-256). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, instructions for use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antibacterial
Indications & Usage
- Hand Sanitizer
Warnings
- For external use only
- Flammable. Keep away from fire or flame.
Otc - When Using
avoid contact with face, eyes, and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Instructions For Use
Wet hands thoroughly with product and rub into skin until dry
Other
Children under 6 years of age should be supervised by an adult when using this product.
Inactive Ingredient
Water (Aqua), Hydroxyethyl Urea, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol, Fragrance (parfume), Red 33 (CI 17200)
Package Label.Principal Display Panel
Back Label (1710712)
Front Label (1710713)
Otc - Questions
1-800-258-3425
Dosage & Administration
Topical liquid
* Please review the disclaimer below.
