Label: PURELL ADVANCED HAND SANITIZER NATURALS FOAM- alcohol liquid

  • NDC Code(s): 21749-875-10, 21749-875-50
  • Packager: GOJO Industries, Inc.
  • 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

If you are a consumer or patient please visit this version.

  • 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

    • Place enough product in your palm to thoroughly cover your hands
    • Run 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, Caprylyl Glycol, Citrus Aurantium Dulcis (Orange) Peel Oil, Glycerin, Lavandula Hybrida (Lavandin) Oil, Litsea Cubeba Fruit Oil, Pelargonium Graveolens (Geranium) Oil, Pogostemon Cablin Oil

  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct LabelProduct LabelProduct LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED HAND SANITIZER NATURALS FOAM 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-875
    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 (UNII: ZEL54N6W95)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ORANGE OIL, COLD PRESSED (UNII: AKN3KSD11B)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAVANDIN OIL (UNII: 9RES347CKG)  
    LITSEA OIL (UNII: 2XIW34BN6O)  
    PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC)  
    POGOSTEMON CABLIN LEAF OIL (UNII: F3IN55X5PO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-875-10295 mL in 1 PACKAGE; Type 0: Not a Combination Product04/15/2021
    2NDC:21749-875-50500 mL in 1 PACKAGE; 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(21749-875) , pack(21749-875) , label(21749-875)