LYSOL TOUCH OF FOAM (BENZALKONIUM CHLORIDE) SOLUTION [RECKITT BENCKISER LLC]

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  • LYSOL TOUCH OF FOAM (BENZALKONIUM CHLORIDE) SOLUTION [RECKITT BENCKISER LLC]

LYSOL TOUCH OF FOAM (BENZALKONIUM CHLORIDE) SOLUTION [RECKITT BENCKISER LLC]
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NDC 63824-466-08, 63824-466-11, 63824-466-25
Set ID 75b10d4f-6adf-4763-b1b8-ccac02f2d6ed
Category HUMAN OTC DRUG LABEL
Packager Reckitt Benckiser LLC
Generic Name
Product Class
Product Number
Application Number PART333E
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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.10%

  • Purpose

    Antibacterial

  • Uses

    for handwashing to decrease bacteria on the skin

  • 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.

  • Directions

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

    store at room temperature

  • 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.

  • Questions? Comments?

    Call 1-800-228-4722

  • SPL UNCLASSIFIED SECTION

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

  • 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)

    creamy
    vanilla
    orchid

    0389679

    PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    LYSOL   TOUCH OF FOAM
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-466
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Lauramine Oxide (UNII: 4F6FC4MI8W)  
    PEG-150 Distearate (UNII: 6F36Q0I0AC)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Coco Monoethanolamide (UNII: C80684146D)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    D&C Green No. 5 (UNII: 8J6RDU8L9X)  
    D&C Red No. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-466-08251 mL in 1 BOTTLE, PUMP
    2NDC:63824-466-11325 mL in 1 BOTTLE, PUMP
    3NDC:63824-466-25739 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E12/26/2012
    Labeler - Reckitt Benckiser LLC (094405024)
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