QS PLUS PLUS INSTANT HAND SANITIZER (BENZEALKONIUM CHLORIDE) LIQUID [ABC COMPOUNDING CO., INC.]

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  • QS PLUS PLUS INSTANT HAND SANITIZER (BENZEALKONIUM CHLORIDE) LIQUID [ABC COMPOUNDING CO., INC.]

QS PLUS PLUS INSTANT HAND SANITIZER (BENZEALKONIUM CHLORIDE) LIQUID [ABC COMPOUNDING CO., INC.]
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NDC 62257-457-10, 62257-457-12, 62257-457-14, 62257-457-15, 62257-457-16, 62257-457-17, 62257-457-18, 62257-457-24, 62257-457-55
Set ID 343f9139-47bc-44b0-9da1-d9d6f6334bc7
Category HUMAN OTC DRUG LABEL
Packager ABC Compounding Co., Inc.
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Drug Facts Box OTC-Active Ingredient Section

    benzalkonium chloride USP 0.13%

  • Drug Facts Box OTC-Indications & Usage Section

    For hand-washing to decrease bacteria on the skin, only when water is not available

  • Drug Facts Box OTC-Warnings Section

    For external use only

  • Drug Facts Box OTC-Purpose Section

    Antiseptic

  • Drug Facts Box-OTC When Using Section

    do not get into eyes

    if contact occurs, rinse eyes thoroughly with water

  • Drug Facts Box-OTC Stop Use Section

    irritation and redness develop

  • Drug Facts Box-OTC Keep Out Of Reach Of Children Section

    If swallowed, get medical help or contact a Poison Control Center right away

  • Drug Facts Box-OTC Dosage & Administration Section

    press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand

    rub hands together until dry

    wash hands with soap and water at earliest opportunity

  • Drug Facts Box-OTC Inactive Ingredient Section

    water, glycerine, dimethicone, DMDM hydantoin, iodopropynl butylcarbamate, methylchloroisothiazolinone, methylisothiazolinone, fragrance

  • QS Plus Plus Instant Hand Sanitizer

    product label

    QS Plus Plus Instant Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    QS PLUS PLUS INSTANT HAND SANITIZER 
    benzealkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62257-457
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62257-457-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product02/20/2019
    2NDC:62257-457-1850 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2019
    3NDC:62257-457-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2019
    4NDC:62257-457-121000 mL in 1 BAG; Type 0: Not a Combination Product02/20/2019
    5NDC:62257-457-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2019
    6NDC:62257-457-16236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2019
    7NDC:62257-457-24115 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2019
    8NDC:62257-457-15946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2019
    9NDC:62257-457-55208200 mL in 1 DRUM; Type 0: Not a Combination Product02/20/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E02/20/2019
    Labeler - ABC Compounding Co., Inc. (003284353)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABC Compounding Co., Inc.003284353manufacture(62257-457)
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