Label: PURELL CS FOAM HANDWASH 2% CHG- chlorhexidine gluconate 2% solution liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated October 26, 2022

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

  • Uses

    Antimicrobial foam handwash

  • Active Ingredient

    Chlorhexidine Gluconate 2%

  • Purpose

    Antiseptic

  • Directions

    Directions

  • Warnings

    For External Use Only

  • Do not use

    if you are allergic to chlorhexidine gluconate or any other ingredients.

  • When using this product

    keep out of eyes, ears, and mouth. May cause serious and permanent eye injury if placed or kept in the eye during surgical procedures or may cause deafness when instilled in the middle of the ear through perforated eardrums. If solution should contact these areas, rinse out promptly and thoroughly with water.

  • Stop use and ask a doctor if

    Irritation, sensitization, or allergic reaction occurs. These may be signs of a serious condition.

  • Keep out of reach of children

    If swallowed, get medical help or contact a poison control center right away.

  • Allergy Alert

    This product may cause a severe allergic reaction. Symptoms may include:

    • wheezing/difficulty breathing
    • shock
    • facial swelling
    • hives
    • rash

    If an Allergic reaction occurs, stop use and seek medical help right away.

  • Inactive Ingredients

    Citric acid, comide DEA, hydroxyethylcellulose, isopropyl alcohol, lauramine oxide. purified water

  • PRINCIPAL DISPLAY PANEL

    Foam Handwash 2% CHG

    Antimicrobial Foam

    Distributed by:

    GOJO Industries, Inc.

    Akron, OH 44309

    +1-330+255-6000

    www.GOJO.com

    ©2022 GOJO Industries, Inc.

    All rights reserved.

    Made in U.S.A.

    Principal Display Panel

    1200mL

    SOAP

    CS6

    GOJOCS6INTLBL

    6581-640-INT-B

  • INGREDIENTS AND APPEARANCE
    PURELL CS FOAM HANDWASH 2% CHG 
    chlorhexidine gluconate 2% solution liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-226
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-226-401200 mL in 1 BOTTLE; Type 0: Not a Combination Product10/13/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only10/13/2022
    Labeler - GOJO Industries, Inc. (004162038)
    Registrant - Xttrium Laboratories, Inc. (007470579)
    Establishment
    NameAddressID/FEIBusiness Operations
    Xttrium Laboratories, Inc.007470579manufacture(21749-226)