Label: PURELL ADVANCED REFRESHING- alcohol gel

  • NDC Code(s): 21749-704-01, 21749-704-02, 21749-704-04, 21749-704-08, view more
    21749-704-10, 21749-704-12, 21749-704-13, 21749-704-15, 21749-704-16, 21749-704-20, 21749-704-24, 21749-704-28, 21749-704-33, 21749-704-45, 21749-704-50, 21749-704-59, 21749-704-65
  • Packager: GOJO Industries, Inc.
  • This is a repackaged label.
  • Source NDC Code(s): 21749-972
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 10, 2024

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  • Active ingredient

    Ethyl alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Uses

    • Hand sanitizer 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 PURELL
  • Inactive ingredients

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

  • PRINCIPAL DISPLAY PANEL

    product label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED REFRESHING 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-704(NDC:21749-972)
    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, D- (UNII: A7E6112E4N)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-704-0129 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2012
    2NDC:21749-704-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2012
    3NDC:21749-704-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2012
    4NDC:21749-704-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2012
    5NDC:21749-704-04118 mL in 1 BOTTLE; Type 0: Not a Combination Product03/15/2012
    6NDC:21749-704-10295 mL in 1 PACKAGE; Type 0: Not a Combination Product03/15/2012
    7NDC:21749-704-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product03/15/2012
    8NDC:21749-704-59591 mL in 1 PACKAGE; Type 0: Not a Combination Product03/15/2012
    9NDC:21749-704-5015 mL in 1 PACKAGE; Type 0: Not a Combination Product03/15/2012
    10NDC:21749-704-45450 mL in 1 PACKAGE; Type 0: Not a Combination Product03/15/2012
    11NDC:21749-704-331000 mL in 1 PACKAGE; Type 0: Not a Combination Product03/15/2012
    12NDC:21749-704-13372 mL in 1 PACKAGE; Type 0: Not a Combination Product05/07/2020
    13NDC:21749-704-16473 mL in 1 PACKAGE; Type 0: Not a Combination Product04/27/2020
    14NDC:21749-704-28828 mL in 1 PACKAGE; Type 0: Not a Combination Product03/15/2020
    15NDC:21749-704-65192 mL in 1 PACKAGE; Type 0: Not a Combination Product06/01/2021
    16NDC:21749-704-24710 mL in 1 PACKAGE; Type 0: Not a Combination Product08/01/2021
    17NDC:21749-704-151500 mL in 1 PACKAGE; Type 0: Not a Combination Product08/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM505G(a)(3)03/15/2012
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534MANUFACTURE(21749-704)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414MANUFACTURE(21749-704) , label(21749-704) , pack(21749-704)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.117959271relabel(21749-704)
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