LYSOL NO TOUCH (BENZALKONIUM CHLORIDE) SOLUTION [RECKITT BENCKISER LLC]

LYSOL NO TOUCH (BENZALKONIUM CHLORIDE) SOLUTION [RECKITT BENCKISER LLC]
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NDC 63824-456-02
Set ID 3653edae-0919-43f4-8227-e25bf57069ff
Category HUMAN OTC DRUG LABEL
Packager Reckitt Benckiser LLC
Generic Name
Product Class
Product Number
Application Number PART333E
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.10%

  • Purpose

    Antibacterial

  • Use

    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

    • Wet hands
    • Place hands under dispenser until soap is dispensed
    • Wash hands
    • Rinse hands with water
    • Dry hands after rinsing
  • Other Information

    store at room temperature

  • Inactive Ingredients

    Water, Cetrimonium Chloride, Glycerin, PEG-150 Distearate, Lauramine Oxide, Cocamide MEA, Fragrance, Citric Acid, Acrylates/PEG-10 Maleate/Styrene Copolymer, Tetrasodium EDTA, Sodium Chloride, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Methylchloroisothiazolinone/ Methylisothiazolinone, PPG-12-Buteth-16

  • Questions? Comments?

    Call 1-800-228-4722

  • SPL UNCLASSIFIED SECTION

    Reckitt Benckiser LLC
    Parsippany, NJ 07054-0224
    Made in U.S.A. © 2012 RB

  • PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

    Aloe Vera &
    Vitamin E
    With Moisturizers

    Lysol®
    BRAND

    KILLS 99.9% OF BACTERIA

    No-Touch
    Refill

    Antibacterial Hand Soap

    0371649

    8.5 FL. OZ. (251 mL)

    Principal Display Panel - 251 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    LYSOL   NO TOUCH
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-456
    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)  
    Cetrimonium Chloride (UNII: UC9PE95IBP)  
    Glycerin (UNII: PDC6A3C0OX)  
    PEG-150 Distearate (UNII: 6F36Q0I0AC)  
    Lauramine Oxide (UNII: 4F6FC4MI8W)  
    Coco Monoethanolamide (UNII: C80684146D)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    PPG-12-Buteth-16 (UNII: 58CG7042J1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-456-02251 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E11/30/2012
    Labeler - Reckitt Benckiser LLC (094405024)

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