Active Ingredient
Ethyl Alcohol, 70%
Kleenex Hand Sanitizer
FDA Label NDC 55118-610
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 (NDC 55118-610). 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, purpose, use, warnings, otc - when using, otc - stop use, otc - 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
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 & consult a health care practitioner if irritation or redness develops or 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
Wet hands thoroughly with product. Rub hands together briskly until dry.
Other Information
Report serious side effects from this product to 1-877-561-6587 Do not store above 37.8 C / 100 F
Inactive Ingredients
Carbopol 1342, Glycerol, Orange Flower Oil, Propylene Glycol, Triethanolamine, Water
Questions?
1-888-346-4652
Principal Display Panel - 50 Ml Bottle Label
Kleenex ® BRAND
Hand Sanitizer Gel
Kills 99.9% of germs
1.7 fl oz / 50 mL
Principal Display Panel (50 mL Bottle Label)
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