Label: LYSOL  TOUCH OF FOAM- benzalkonium chloride solution 

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

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 11/12

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

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  • Active Ingredient

    Benzalkonium Chloride 0.10%

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  • Purpose

    Antibacterial

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  • Uses

    for handwashing to decrease bacteria on the skin

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  • Warnings

    For external use only

    When using this product

    • Avoid contact with eyes.
    • In case of eye contact, flush with water.

    Stop use and ask a doctor if irritation or redness develops.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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  • Directions

    • Apply product to hands.
    • Wash hands.
    • Rinse hands with water.
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  • Other Information

    store at room temperature

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  • Inactive Ingredients

    Water, Glycerin, Lauramine Oxide, PEG-150 Distearate, Cetrimonium Chloride, Propylene Glycol, Fragrance, Citric Acid, Tetrasodium EDTA, Cocamide MEA, Methylchloroisothiazolinone, Methylisothiazolinone, D&C Green No. 5, D&C Red No. 33.

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  • Questions? Comments?

    Call 1-800-228-4722

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  • SPL UNCLASSIFIED SECTION

    Distributed by: Reckitt Benckiser LLC
    Parsippany, NJ 07054-0224
    Made in U.S.A.

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  • PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

    new

    Lysol®
    BRAND
    KILLS 99.9% OF BACTERIA

    Touch of
    Foam
    ANTIBACTERIAL
    HAND WASH

    8.5 FL. OZ.
    (251 mL)

    wild
    berry bliss

    0389682

    PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label
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  • INGREDIENTS AND APPEARANCE
    LYSOL   TOUCH OF FOAM
    benzalkonium chloride solution
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:63824-467
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Benzalkonium Chloride (Benzalkonium) Benzalkonium Chloride 0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water  
    Glycerin  
    Lauramine Oxide  
    PEG-150 Distearate  
    Cetrimonium Chloride  
    Propylene Glycol  
    Citric Acid Monohydrate  
    Edetate Sodium  
    Coco Monoethanolamide  
    Methylchloroisothiazolinone  
    Methylisothiazolinone  
    D&C Green No. 5  
    D&C Red No. 33  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63824-467-08 251 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part333E 12/26/2012
    Labeler - Reckitt Benckiser LLC (094405024)
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