Label: PURELL ADVANCED HAND SANITIZER MOISTURIZING 2IN1 FOAM- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated April 15, 2021

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  • Active ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use

    • 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

    • 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

  • Inactive ingredients

    Water (Aqua), Isopropyl Alcohol, PEG-12 Dimethicone, Avena Sativa (Oat) Kernel Extract, Canarium Luzonicum Gum Nonvolatiles, Caprylyl glycol, Citrus Aurantifolia (Lime) Peel Oil, Citrus Aurantium Bergamia (Bergamot) Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Glycerin, Isopropyl Myristate, Litsea Cubeba Fruit Oil, Mentha Arvensis Leaf Oil, Mentha Viridis (Spearmint) Leaf Oil, Niaciniamide, Pinus Silvestrus Leaf Oil, Pogostemon Cablin Oil, PPG-12/SMDI copolymer, Schinus Molle Oil, Tocopheryl Acetate, Potassium Sorbate

  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED HAND SANITIZER MOISTURIZING 2IN1 FOAM 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-851
    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)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    OAT (UNII: Z6J799EAJK)  
    ELEMI (UNII: C13XI009KO)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    LIME OIL (UNII: UZH29XGA8G)  
    BERGAMOT OIL (UNII: 39W1PKE3JI)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LEMON OIL (UNII: I9GRO824LL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Isopropyl Myristate (UNII: 0RE8K4LNJS)  
    LITSEA OIL (UNII: 2XIW34BN6O)  
    MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)  
    SPEARMINT OIL (UNII: C3M81465G5)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)  
    PATCHOULI OIL (UNII: F3IN55X5PO)  
    PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)  
    SCHINUS MOLLE FRUIT OIL (UNII: 99O5U5NLK2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-851-10295 mL in 1 BOTTLE; Type 0: Not a Combination Product04/15/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/15/2021
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-851) , pack(21749-851) , label(21749-851)
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