Label: OVATION INSTANT HAND SANITIZER- benzethonium chloride liquid

  • NDC Code(s): 67858-001-01, 67858-001-50
  • Packager: QuestSpecialty Corporation
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 12, 2024

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  • Active Ingredient

    Benzenethonium chloride USP 0.2%

  • Purpose

    Sanitizer

  • Uses

    Handwash to help decrease bacteria on the skin.

    Recommended for repeated use.

  • Warnings

    For external use only

  • Do Not Use

    In the eyes.

  • When using this product

    Do not get in eyes. If contact occurs, flush eyes with water and contact a doctor immediately. If swallowed, seek medical attention.

  • Stop use and ask a doctor if

    Skin irritation develops.

  • Directions

    Press dispenser twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand. Rub hands together until hands are dry. Wash with soap and water at earliest opportunity.

  • Keep out of reach of children

    Children under 6 years old should be supervised  by an adult when using this product   

  • Other Information

    Store at room temperature

  • Inactive Ingredients

    Water, glycerin, dimethicone, DMDM Hydantoin, Iodopropynyl butylcarbamate, fragrance, hydroxythyl cellulose.

  • Label Image

    image description

  • INGREDIENTS AND APPEARANCE
    OVATION  INSTANT HAND SANITIZER
    benzethonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67858-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE1 mg  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67858-001-0112 in 1 CARTON04/01/201105/31/2021
    1NDC:67858-001-5050 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/01/201105/31/2021
    Labeler - QuestSpecialty Corporation (103840377)
    Registrant - QuestSpecialty Corporation (103840377)
    Establishment
    NameAddressID/FEIBusiness Operations
    QuestSpecialty Corporation103840377manufacture(67858-001)
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