Label: PURELL- alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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  • Drug Facts

  • Active ingredient 

    Ethyl Alcohol 70% v/v

    Purpose

    Antimicrobial

  • Uses

    • Hand sanitized to help reduce bacteria on the skin
  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.

    When using this product

    do not 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 appears and lasts

    Keep out of reach of children.

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

  • Directions

    • Put enough product in your palm to cover hands and rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product
  • Other information

    • Store below 110°F (43°C)
    • May discolor certain fabrics or surfaces
  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30, Alkly Acrylate, Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum)

  • Questions?

    1-888-4-PURELL www.PURELL.com

  • Purell, 1oz

    Label4

  • Purell, 2oz

    Label5

  • INGREDIENTS AND APPEARANCE
    PURELL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-188(NDC:21749-704)
    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)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67751-188-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product12/04/2017
    2NDC:67751-188-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product12/04/201709/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/04/2017
    Labeler - Navajo Manufacturing Company Inc. (091917799)
    Registrant - Navajo Manufacturing Company Inc. (091917799)
    Establishment
    NameAddressID/FEIBusiness Operations
    Navajo Manufacturing Company Inc.136941411relabel(67751-188) , repack(67751-188)
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