Label: LYSOL NO-TOUCH- 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 December 3, 2013

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  • 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, Citric Acid, Fragrance,Tetrasodium EDTA, Sodium Chloride, Methylchloroisothiazolinone/ Methylisothiazolinone, PPG-12-Buteth-16, FD&C Blue #1

  • Questions? Comments?

    Call 1-800-228-4722

  • SPL UNCLASSIFIED SECTION

    Made in U.S.A.

  • PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

    Limited Edition

    Sensitive
    Skin

    Dermatologically
    Tested

    Lysol®
    BRAND
    KILLS 99.9% OF BACTERIA

    No-Touch™
    Refill

    Antibacterial Hand Soap

    Paraben Free • Triclosan Free

    8.5 FL. OZ. (251 mL)

    8105848

    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:63824-479
    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)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    PPG-12-Buteth-16 (UNII: 58CG7042J1)  
    FD&C Blue No. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-479-02251 mL in 1 BOTTLE
    2NDC:63824-479-011 in 1 BLISTER PACK
    2251 mL in 1 BOTTLE, PLASTIC
    3NDC:63824-479-033 in 1 BLISTER PACK
    3251 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E12/01/2013
    Labeler - Reckitt Benckiser LLC (094405024)
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