Label: HAND SANITIZER WITH ALOE- 65% ethyl alcohol gel

  • NDC Code(s): 59958-500-02
  • Packager: Owen Biosciences, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2024

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

  • Drug Facts

    Active Ingredients Purpose
    Ethyl Alcohol 65% v/v....................Antimicrobial

    Use

    ■ Hand sanitizer to help reduce bacteria on the skin

    Use

    ■ Hand sanitizer to help reduce bacteria on the skin

    Warnings

    ■ For external use only.
    ■ When using this product avoid use in or near the
    eyes. In case of contact, rinse eyes thoroughly with
    water.
    ■ Stop use and ask a doctor if irritation or rash occurs.
    ■ Keep out of reach of children. If swallowed, get
    medical help or contact Poison Control.

    ■ Flammable. Keep away from fire and flame.

    warnings

    ■ For external use only.
    ■ When using this product avoid use in or near the
    eyes. In case of contact, rinse eyes thoroughly with
    water.
    ■ Stop use and ask a doctor if irritation or rash occurs.
    ■ Keep out of reach of children. If swallowed, get
    medical help or contact Poison Control.

    ■ Flammable. Keep away from fire and flame.

    Directions

    ■ Apply product generously in palm using enough to
    cover hands. Rub hands together until dry. Children
    under 6 years of age should be supervised when using
    this product.

    Other information

    ■ Protect the product in this container from excessive
    heat and direct sun. Store below 110ºF(43ºC).
    ■ May discolor some fabrics or surfaces

    Inactive ingredients

    Water, Hydroxyethylcellulose,
    Glycerin, Menthol, Cocoyl Argininamide, Safflower Acids,
    Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Coconut
    Acids, Eucalyptus Globulus Leaf Oil, Caprylyl Glycol,
    Fragrance, 1,2-Hexanediol, Disodium EDTA-Copper

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  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER WITH ALOE 
    65% ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59958-500
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 30 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59958-500-0218500 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/23/2020
    Labeler - Owen Biosciences, Inc. (790003045)
    Registrant - Owen Biosciences, Inc. (790003045)