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Drug Facts
Distributed in the U.S. by
Kimberly-Clark Global Sales,
LLC, Roswell, GA 30076-2199
Kleenex Hand Sanitizer, Green Certified
FDA Label NDC 55118-535
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 Hand Sanitizer, Green Certified (NDC 55118-535). 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 70%
Purpose
Antimicrobial
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 immediately.
Directions
Use enough foam to cover your hands. Rub hands together briskly until 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
Aloe Barbadensis Leaf Extract, Betaine, Camellia Oleifera Leaf Extract, Citric Acid, Cucumis Sativus (Cucumber) Fruit Extract, Isopropanol, Glycerin, Meadowfoamamidopropyl Betaine, Panthenol, PEG-10 Dimethicone, Water
Questions?
1-888-346-4652
Principal Display Panel - 236 Ml Bottle Label
Kleenex®
BRAND
Foam
Hand Sanitizer
green
certified
CERTIFIED
EcoLogo®
Certified Instant
Hand Antiseptic
CCD-170
8 fl oz (236 mL)
20-14-611-0-00
Principal Display Panel (236 mL Bottle Label)
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