Label: HAND SANITIZER ORANGE BLOSSOM- ethyl alcohol spray

  • NDC Code(s): 42681-0007-2
  • Packager: Whole Foods Market, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 2, 2024

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  • ACTIVE INGREDIENT

    Active ingredient Purpose

    Ethyl Alcohol 62% Antiseptic

  • PURPOSE

    Uses ■ to help reduce bacteria on the skin.

  • WARNINGS

    For external use only. Flammable. Keep away from fire or flame.

  • WHEN USING

    When using this product avoid contact with eyes. If eye contact occurs, rinse with water.

  • STOP USE

    Stop use and ask a doctor if skin irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions ■ apply 1 to 2 sprays on hands and rub together until dry

  • INDICATIONS & USAGE

  • STORAGE AND HANDLING

    Do not store above 104F (40C)

  • INACTIVE INGREDIENT

    Inactive ingredients water, isopropyl alcohol, fragrance (natural)*, glycerin, helianthus annuus (sunflower) seed oil, rosmarinus

    officinalis (rosemary) leaf extract, triethyl citrate.

  • QUESTIONS

    Questions, Comments? ■ customer.questions@wholefoods.com ■ 1-844-936-8255

  • PRINCIPAL DISPLAY PANEL

    OBHS2DFOBHS2F

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  ORANGE BLOSSOM
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42681-0007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ROSEMARY (UNII: IJ67X351P9)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42681-0007-259 mL in 1 BOTTLE; Type 0: Not a Combination Product10/09/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/09/2023
    Labeler - Whole Foods Market, Inc. (196175616)
    Registrant - KDC/ONE SOCAL LABORATORIES, LLC (118384240)
    Establishment
    NameAddressID/FEIBusiness Operations
    KDC/ONE SOCAL LABORATORIES, LLC118384240manufacture(42681-0007)
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