PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]

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PURE FORCE (BENZALKONIUM CHLORIDE) LIQUID [ECOLAB INC.]
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NDC 47593-504-41, 47593-504-59
Set ID 66fd73be-05c8-4905-96f5-f73fa1447b3f
Category HUMAN OTC DRUG LABEL
Packager Ecolab Inc.
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Active Ingredient

    Benzalkonium chloride 0.1%

  • Purpose

    Antiseptic handwash

  • Uses

    • for handwashing to decrease bacteria on the skin
    • recommended for repeated use
  • Warnings

    • For external use only

    Do not use

    • In eyes

    When using this product

    • If in eyes, rinse promptly and thoroughly with water
    • discontinue use if irritation and redness develop

    Stop use and ask a doctor if skin irritation or redness occurs 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

    • wash hands to remove soil
    • dispense palmful
    • spread to cover hands, rub in well
    • air dry, do not rinse or towel dry
  • Other information

    • for additional information, see Material Safety Data Sheet (MSDS)
    • for emergency medical information in USA, call 1.800.328.0026
  • INACTIVE INGREDIENT

    Inactive ingredients  water (aqua), isopropoyl alcohol, propylene glycol, FDC red 40, FDC blue 1

  • QUESTIONS

    Questions? call 1.866.444.7450

  • Principal Display Panel with Representative Label

    Hand Sanitizing Foam

    Active ingredient:  Benzalkonium chloride 0.1%

    25 FL OZ (750 mL)

    Pure Force™

    Distributed by:                        © 2013 Ecolab USA Inc.

    PureForce                               All Rights Reserved

    370 Wabasha Street North       Made in U.S.A.

    St. Paul, MN 55102                           755509/7100/0713

    representative label

  • INGREDIENTS AND APPEARANCE
    PURE FORCE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-504
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47593-504-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/28/2013
    2NDC:47593-504-591250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/28/201309/28/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/28/2013
    Labeler - Ecolab Inc. (006154611)
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