Label: PUREFORCE- alcohol solution

  • 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 June 1, 2023

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  • Active ingredient

    Ethanol, 60% by volume

  • Purpose

    Antiseptic handwash

  • Uses

    • for handwashing to decrease bacteria on the skin
  • Warnings

    • For external use only
    • FLAMMABLE.  Keep away from sparks and open flame.

    Do not use

    • in eyes
    • on deep cuts or puncture wounds

    When using this product

    • if in eyes, promptly and throughly with water
    • discontinue use if irritation and redness develop

    Stop use and ask a doctor if

    • eye or skin irritation and redness persist for more than 72 hours

    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • apply liberal amount into hand
    • spread by rubbing hands together
    • rub to dryness with attention to area around nails and between fingers
  • INACTIVE INGREDIENT

    Inactive ingredients  water, isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

  • Other information

    • THIS PRODUCT IS NOT A SUBSTITUTE FOR HANDWASHING WITH SOAP AND WATER
    • for additional information, see Material Safety Data Sheet (MSDS)
    • for emergency medical information in USA and Canada, call 1.800.328.0026
    • For emergency medical information worldwide, call 1.651.222.5352 (in USA)
  • QUESTIONS

    Questions? call 1.866.444.7450

  • Principal display panel and representative label

    PureForce

    Hand Sanitizer

    Hand Care

    G

    Use  Pureforce Hand Sanitizer to sanitize hands

    between handwashings.

    Product No.

    8000055

    Net Contents: 27 fl oz/800 mL

    For questions or comments,

    call 1-866-444-7450

    www.pureforcesvc.com

    Distribute by:

    PureForce

    370 Wabasha Street North

    St. Paul, MN 55102

    copyright 2010 PureForce

    All Rights Reserved

    Made in U.S.A.

    749946/7100/0610

    representative label

  • INGREDIENTS AND APPEARANCE
    PUREFORCE 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-473
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MYRISTYL ALCOHOL (UNII: V42034O9PU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-473-25800 mL in 1 POUCH; Type 0: Not a Combination Product04/27/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/27/2011
    Labeler - Ecolab Inc. (006154611)
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