Label: PURELL ADVANCED HAND SANITIZER NATURALS GEL- alcohol gel

  • NDC Code(s): 21749-625-01, 21749-625-02, 21749-625-04, 21749-625-08, view more
    21749-625-10, 21749-625-12, 21749-625-24, 21749-625-28, 21749-625-29, 21749-625-65
  • 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 May 19, 2021

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

View All Sections
  • 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

    • Put enough product in your palm to cover hands and rub hands together briskly until dry
    • Children under 6 yeasr of age should be supervised when using PURELL
  • Inactive Ingredients:

    Water (Aqua), Isopropyl Alcohol, Caprylyl glycol, Citrus Aurantium Dulcis (Orange) Peel Oil, Glycerin, Isopropyl Myristate, Lavandula Hybrida (Lavandin) oil, Litsea Cubeba Fruit Oil, Pelargonium Graevolens (Geranium) oil, Pogostemon Cablin Oil, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol

  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    PURELL ADVANCED HAND SANITIZER NATURALS GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-625
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    BITTER ORANGE OIL (UNII: 9TLV70SV6I)  
    LAVANDIN OIL (UNII: 9RES347CKG)  
    LITSEA OIL (UNII: 2XIW34BN6O)  
    GERANIUM OIL, ALGERIAN TYPE (UNII: 5Q1I94P4WG)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PATCHOULI OIL (UNII: F3IN55X5PO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-625-0130 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
    2NDC:21749-625-0259 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
    3NDC:21749-625-04118 mL in 1 PACKAGE; Type 0: Not a Combination Product12/15/2019
    4NDC:21749-625-08236 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
    5NDC:21749-625-29295 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
    6NDC:21749-625-12355 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
    7NDC:21749-625-28828 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
    8NDC:21749-625-101000 mL in 1 PACKAGE; Type 0: Not a Combination Product01/01/2016
    9NDC:21749-625-24710 mL in 1 PACKAGE; Type 0: Not a Combination Product08/01/2021
    10NDC:21749-625-65192 mL in 1 PACKAGE; Type 0: Not a Combination Product07/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2016
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-625)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.088312414manufacture(21749-625) , label(21749-625) , pack(21749-625)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!