Label: DR. HESS HAND SANITIZER- alcohol gel

  • NDC Code(s): 79346-101-01, 79346-101-02, 79346-101-03, 79346-101-04, view more
    79346-101-07, 79346-101-08
  • Packager: Dr. Hess Wellness Corp.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 18, 2023

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  • Active Ingredients

    Ethyl Alcohol 70%.

  • Purpose

    Antibacterial

  • Use

    For rinse-free hand sanitizing to remove 99.9% bacteria on skin.

  • Warnings

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

    When using this product

    Do not use in eyes. In case of contact with eyes, rinse with water.

    Stop use and ask a doctor if

    irritation and redness develop and persist.

    Keep out of reach of children.

    If swallowed, get medical help promptly.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Other Information

    Store under 105°F

  • Inactive Ingredients

    Water, Acrylates Copolymer, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

  • Principal Display Panel – Bottle Label

    Kills
    99.9%
    of Germs

    Dr. Hess
    1893

    Ashland, Ohio

    Dr. Hess
    Hand
    Sanitizer

    70% Alcohol

    Anti-Bacterial Hand Gel

    8 fl oz (236 ml)

    Principal Display Panel – Bottle Label
  • INGREDIENTS AND APPEARANCE
    DR. HESS HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79346-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Butyl Acrylate/Methyl Methacrylate/Methacrylic Acid Copolymer (18000 MW) (UNII: JZ1374NL9E)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Glycerin (UNII: PDC6A3C0OX)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked) (UNII: 59TL3WG5CO)  
    Aminomethylpropanol (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79346-101-0159 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202012/31/2020
    2NDC:79346-101-02118 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202012/31/2020
    3NDC:79346-101-03236 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202012/31/2020
    4NDC:79346-101-04473 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202012/31/2020
    5NDC:79346-101-073785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/01/202012/14/2024
    6NDC:79346-101-084 in 1 BOX07/01/202012/14/2024
    63785 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/01/202012/14/2024
    Labeler - Dr. Hess Wellness Corp. (117544756)
    Establishment
    NameAddressID/FEIBusiness Operations
    Fresh & Beautiful Cosmetics117409349MANUFACTURE(79346-101)
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