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

LYSOL NO-TOUCH (BENZALKONIUM CHLORIDE) SOLUTION [RECKITT BENCKISER LLC]
PDF | XML

NDC 63824-476-01, 63824-476-02
Set ID 8dd28e5f-3140-4771-acae-8a5b53e9c9c4
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 hand washing 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, Methylchloroisothiazolinone/Methylisothiazolinone, PPG-12-Buteth-16, FD&C Yellow No. 5, D&C Orange No. 4, D&C Red No. 33, FD&C Blue No. 1.

  • Questions? Comments?

    Call 1-800-228-4722

  • SPL UNCLASSIFIED SECTION

    Made in U.S.A.

  • PRINCIPAL DISPLAY PANEL - 251 mL Bottle Label

    Vanilla Sugar
    & Spice

    LIMITED HOLIDAY COLLECTION

    Lysol®
    BRAND
    KILLS 99.9% OF BACTERIA

    No -Touch
    Antibacterial
    Hand Soap Refill

    8.5 FL. OZ. (251 mL)

    0344480

    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:63824-476
    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)  
    Methacrylate/Methoxy Peg-10 Maleate/Styrene Copolymer (UNII: 39DK5WQ2PR)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    PPG-12-Buteth-16 (UNII: 58CG7042J1)  
    FD&C Yellow No. 5 (UNII: I753WB2F1M)  
    D&C Orange No. 4 (UNII: Q1LIY3BO0U)  
    D&C Red No. 33 (UNII: 9DBA0SBB0L)  
    FD&C Blue No. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-476-011 in 1 BLISTER PACK
    1251 mL in 1 BOTTLE
    2NDC:63824-476-02200 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E01/23/2013
    Labeler - Reckitt Benckiser LLC (094405024)

Related Drugs