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Kay Foaming Hand Sanitizer (Kay Chemical Company)

Available Formats

Dosage Form Package Information Links
SOLUTION 750 mL in 1 BOTTLE, PLASTIC (63146-109-03) Label Information
SOLUTION 1200 mL in 1 BOTTLE, PLASTIC (63146-109-06) Label Information

Complete Kay Foaming Hand Sanitizer Information

  • Active ingredient

    Benzalkonium chloride 0.1%


  • Purpose

    Antiseptic handwash


  • Uses

    • For handwashing to decrease bacteria on the skin

  • Warnings

    For external use only

    Do not use
    • In eyes

    When using this product
    • if in eyes, rinse promptly and thoroughly with water
    • discontinue use if irritation and redness develop

    Stop use and ask a doctor if
    • skin irritation and redness occurs for more than 72 hours

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.


  • Directions

    • wash hands to remove soil
    • dispense palmful
    • spread to cover hands, rub in well
    • air dry, do not rinse or towel dry

  • Other Information

    • for additional information, see Safety Data Sheet (SDS)
    • Medical emergency:  (877) 231-2615 or call collect 0 (952) 853-1713

  • INACTIVE INGREDIENT

    Inactive ingredients  water (aqua), isopropyl alcohol, propylene glycol, FDC Red 40, FDC Blue 1


  • QUESTIONS

    Questions?  Call 1-800-529-5458


  • Principal Display Panel and representative label

    NDC 63146-109-08

    KAY

    Foaming Hand Sanitizer

    KEEP OUT OF REACH OF CHILDREN - FOR INSTITUTIONAL USE ONLY

    Benzalkonium chloride 0.1%

    See inside the back label for complete drug facts panel

    To obtain Spanish Instructions, see outer carton

    Net contents: 25 US fl oz (750 ml)

    Distributed by:

    Kay Chemical Company  8300 Capital Drive

    Greensboro, NC 27409-9790  USA

    Customer Service: (800) 529-5458

    ©2013 Kay Chemical Company | All rights reserved

    756217-00 KUSA 756217/8000/0813

    representative label


  • INGREDIENTS AND APPEARANCE
    KAY 
    benzalkonium chloride solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-109
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:63146-109-03 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/22/2008
    2 NDC:63146-109-06 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/22/2011
    3 NDC:63146-109-10 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/10/2014
    4 NDC:63146-109-08 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/10/2014
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 02/22/2008
    Labeler - Kay Chemical Company (003237021)