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

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LYSOL NO-TOUCH (BENZALKONIUM CHLORIDE) KIT [RECKITT BENCKISER LLC]
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NDC 63824-488-01, 63824-489-02, 63824-493-03
Set ID c5289e97-7bae-40c0-9382-eb4634b98bbf
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

    Odor Neutralizing Lemon & Verbena

    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, Propylene Glycol, Citric Acid, Fragrance, Tetrasodium EDTA, Sodium Chloride, Hydrolyzed Collagen, PPG-12-Buteth-16, Magnesium Nitrate, Butylene Glycol, Phenoxyethanol, Methylchloroisothiazolinone, Magnesium Chloride, Ethylhexylglycerin, Methylisothiazolinone, FD&C Yellow No. 5, FD&C Yellow No. 6.

  • Questions? Comments?

    Call 1-800-228-4722

  • SPL UNCLASSIFIED SECTION

    Moisturizing Aloe & Vitamin E

    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, Propylene Glycol, Citric Acid, Tetrasodium EDTA, Acrylates/PEG-10 Maleate/Styrene Copolymer, Sodium Chloride, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Hydrolyzed Collagen, PPG-12-Buteth-16, Magnesium Nitrate, Butylene Glycol, Phenoxyethanol, Methylchloroisothiazolinone, Magnesium Chloride, Ethylhexylglycerin, Potassium Sorbate, Methylisothiazolinone, Sodium Benzoate.

  • Questions? Comments?

    Call 1-800-228-4722

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - Kit Carton

    Lysol®
    BRAND
    KILLS 99.9% OF BACTERIA

    Antibacterial Hand Soap

    No-Touch®
    Hand Soap System
    Helps stop the spread of bacteria

    Refill 3-Pack

    TOTAL:
    25.5 FL. OZ.
    (753 mL)

    EACH:
    8.5 FL. OZ.
    (251 mL)

    PRINCIPAL DISPLAY PANEL - Kit Carton
  • INGREDIENTS AND APPEARANCE
    LYSOL  NO-TOUCH
    benzalkonium chloride kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63824-493
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-493-031 in 1 CARTON
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 12 BOTTLE 502 mL
    Part 21 BOTTLE 251 mL
    Part 1 of 2
    LYSOL  NO-TOUCH
    benzalkonium chloride solution
    Product Information
    Item Code (Source)NDC:63824-488
    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)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-488-01251 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/07/2015
    Part 2 of 2
    LYSOL  NO-TOUCH
    benzalkonium chloride solution
    Product Information
    Item Code (Source)NDC:63824-489
    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)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PPG-12-BUTETH-16 (UNII: 58CG7042J1)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63824-489-02251 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/21/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/08/2015
    Labeler - Reckitt Benckiser LLC (094405024)
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