Label: PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT- benzalkonium chloride wipe cloth

  • NDC Code(s): 21749-359-10, 21749-359-15, 21749-359-20, 21749-359-40
  • 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 February 24, 2022

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

View All Sections
  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help reduce bacteria on the skin

  • Warnings

    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

    • Wet hands thoroughly with product and allow to dry

    • Children under 6 years of age should be supervised when using PURELL

  • Inactive ingredients

    Water (Aqua), Decyl Glucoside, Glycerin, Fragrance(Parfum), Phenoxyethanol

  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    PURELL HAND SANITIZING WIPES CLEAN REFRESHING SCENT 
    benzalkonium chloride wipe cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-359
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-359-1010 in 1 PACKAGE08/01/2014
    137 mL in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:21749-359-1515 in 1 PACKAGE08/01/201402/02/2020
    264 mL in 1 PACKAGE; Type 0: Not a Combination Product
    3NDC:21749-359-2020 in 1 PACKAGE08/01/2014
    374 mL in 1 PACKAGE; Type 0: Not a Combination Product
    4NDC:21749-359-4040 in 1 PACKAGE08/01/2014
    4173 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/01/2014
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534manufacture(21749-359)
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!