Label: MEDICHOICE INSTANT HAND SANITIZER FRAGRANCE FREE- alcohol gel

  • NDC Code(s): 39892-0401-2, 39892-0401-3
  • Packager: Owens & Minor Distribution, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2024

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70% v/v

    Purpose

    Antiseptic

  • Uses

    • hand sanitizer to help reduce bacteria  on the skin
  • Warnings

    Flammable. Keep away from fire or flame

    For external use only - hands.

    Do not use

    in or near the eyes. In case of contact, rinse eyes thoroughly with water

    Stop use and ask a doctor

    if skin irritation and redness or rash develops.

    Keep out of reach of children.

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

  • Directions

    • place enough product in your palm to thoroughly cover your hands
    • rub hands together briskly until dry
    • children under 6 years of age should be supervised when using this product
    • not recommended for infants
  • Other Information

    • store at normal room temperature 
    • may discolor certain fabrics
    • may be harmful to wood finishes and plastics
  • Inactive ingredients

    Purified Water, Isopropyl Alcohol, Propylene Glycol, Aloe Barbadensis Leaf Juice (Decolorized), Carbomer, Glycerin, Aminomethyl Propanol, Isopropyl Myristate, Tocopheryl Acetate

  • Package Labeling: (39892-0401-2) 

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  • Package Labeling: (39892-0401-3)

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  • INGREDIENTS AND APPEARANCE
    MEDICHOICE INSTANT HAND SANITIZER  FRAGRANCE FREE
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39892-0401
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:39892-0401-2118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/21/2019
    2NDC:39892-0401-3237 mL in 1 BOTTLE; Type 0: Not a Combination Product01/21/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/21/2019
    Labeler - Owens & Minor Distribution, Inc. (847412269)
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