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Drug Facts
Distributed in the U.S. by
Kimberly-Clark
Global Sales, LLC, Roswell,
GA 30076-2199
Kleenex Instant Hand Sanitizer
FDA Label NDC 55118-704
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kimberly-clark Corporation for the product Kleenex Instant Hand Sanitizer (NDC 55118-704). 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 other, active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - 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 68% v/v
Purpose
Antiseptic
Use
Hand sanitizer to decrease bacteria on the skin.
Warnings
Flammable - Keep product away from fire or flame.
For External Use Only.
Otc - When Using
When using this product avoid contact with eyes; in case of contact, flush eyes with water.
Otc - Stop Use
Stop use & ask a doctor if irritation or redness develops and persists.
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 allow to dry.
Other Information
- Report serious side effects from this product to 1-877-561-6587.
- Do not store above 110°F (40°C).
Inactive Ingredients
Water, Carbomer, Fragrance, Aminomethyl Propanol, Glycerin
Questions?
1-888-346-4652
Principal Display Panel - 236 Ml Bottle Label
Kleenex®
BRAND
Instant Hand
Sanitizer
kills
germs†
8 fl oz (236 mL)
20-14-141-0-08
Principal Display Panel (236 mL Bottle Label)
* Please review the disclaimer below.
