Label: KLEENEX ANTIMICROBIAL FOAM SKIN CLEANSER- benzalkonium chloride solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 16, 2019

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  • SPL UNCLASSIFIED SECTION
    Drug Facts
  • Active Ingredient
    Benzalkonium Chloride 0.1% w/w
  • Purpose
    Antiseptic cleanser
  • Use
    For personal hand hygiene to help prevent the spread of certain bacteria.
  • Warnings
    For External Use Only. Do not ingest - Use with caution in children - When using this product avoid contact with eyes; in case of contact, flush eyes with water. Discontinue use and ...
  • Directions
    Apply a small amount and lather hands in water for at least 30 seconds. Rinse well. Adults: Supervise children when using this product. Do not dilute product. For occasional use as needed.
  • Other Information
    Report serious side effects from this product to 1-877-561-6587.
  • Inactive Ingredients
    Aloe Barbadensis Leaf Juice Powder, Citric Acid, Coco-Betaine, Glycerin, Panthenol, Sodium Benzoate, Sodium Chloride, Sodium Hydroxide, Tocopheryl Acetate, Water.
  • Questions?
    1-888-346-4652
  • SPL UNCLASSIFIED SECTION
    Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199. Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5.
  • PRINCIPAL DISPLAY PANEL - 50.7 fl oz Bottle Label
    Kleenex® BRAND Antimicrobial Foam - Skin Cleanser - Benzalkonium Chloride Solution, NF - new active ingredient - Benzalkonium - Chloride - DIN: 02443244 - For Personal / Domestic Use Only - 1.5 ...
  • INGREDIENTS AND APPEARANCE
    Product Information
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