Label: QS PLUS INSTANT HAND SANITIZER- benzethonium chloride liquid

  • 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 October 24, 2018

If you are a consumer or patient please visit this version.

  • Drug Facts Box OTC-Active Ingredient Section

    benzethonium chloride USP 0.2%

  • 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, fragrance

  • QS Plus Instant Hand Sanitizer

    product label

    QS Plus Instant Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    QS PLUS INSTANT HAND SANITIZER 
    benzethonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13302-575
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE2 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)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13302-575-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/24/2018
    2NDC:13302-575-121000 mL in 1 BAG; Type 0: Not a Combination Product10/24/2018
    3NDC:13302-575-13800 mL in 1 BAG; Type 0: Not a Combination Product10/24/2018
    4NDC:13302-575-1850 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/24/2018
    5NDC:13302-575-27800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product10/24/2018
    6NDC:13302-575-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/24/2018
    7NDC:13302-575-16236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/24/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/24/2018
    Labeler - Romaine Companies (929229797)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABC Compounding Co., Inc.003284353manufacture(13302-575)