Label: MEDICHOICE INSTANT HAND SANITIZER HONEY SCENTED- alcohol gel

  • NDC Code(s): 39892-0400-1, 39892-0400-2
  • Packager: Owens & Minor Distribution, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 9, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • 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, Fragrance, Aloe Barbadensis Leaf Juice (Decolorized), Carbomer, Glycerin, Aminomethyl Propanol, Isopropyl Myristate, Tocopheryl Acetate

  • Package Labeling: (39892-0400-1)

    Tube

  • Package Labeling: (39892-0400-2)

    Tube 2

  • INGREDIENTS AND APPEARANCE
    MEDICHOICE INSTANT HAND SANITIZER   HONEY SCENTED
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39892-0400
    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:39892-0400-1118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/21/2019
    2NDC:39892-0400-2237 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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!