Label: INSTANT HAND SANITIZER UNSCENTED- alcohol gel

  • NDC Code(s): 65626-470-16
  • Packager: Hu-Friedy Mfg. Co., Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Uses

    • hand sanitizer to help reduce bacteria on the skin that could cause disease
  • Warnings

    Flammable. Keep away from fire or flame

    For external use only - hands.

    When using this productdo not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a physician ifskin irritation or rash develops.

    Keep out of reach of children.If accidently ingested, seek medical help or contact a Poison Control Center immediately.

  • 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
  • Other Information

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

    carbomer, glycerin, isopropyl alcohol, isopropyl myristate, propylene glycol, purified water, tocopheryl acetate, aloe vera gel, AMP-95

  • SPL UNCLASSIFIED SECTION

    MFG BY: HYDROX LABORATORIES
    825 Tollgate Road ELGIN, IL 60123

  • PRINCIPAL DISPLAY PANEL 

    NDC 65626-470-16

    Instant
    Hand
    Sanitizer

    with Moisturizers
    Aloe & Vitamin E

    KILLS 99.9%

    OF GERMS*

    IMS-1505-2

    16 fl oz (473 mL)

    *Effective at eliminating 99.9% of many common harmful germs and bacteria.

    HuFriedyGroup

    The Best In Practice

    4oz Label

  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER UNSCENTED 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65626-470
    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
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65626-470-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/26/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/26/2021
    Labeler - Hu-Friedy Mfg. Co., Inc. (005085972)
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