Label: CLEAN CHOICE ALCOHOL SANITIZER- alcohol liquid 

  • Label RSS
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 09/13

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

  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl Alcohol 70% ww

    Close
  • PURPOSE

    Purpose

    Antibacterial

    Close
  • INDICATIONS & USAGE

    Uses

    For hand sanitizing to reduce bacteria on the skin

    Close
  • WARNINGS

    Warnings

    For external use only

    Flammable: Keep away from fire or flame.

    When using this product avoid contact with eyes.  In case of eye contact, flush with water.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

    Close
  • DOSAGE & ADMINISTRATION

    Directions

    Apply foaming sanitizer to cover hands

    Rub into skin

    No rinsing required

    Close
  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Bis-PEG-12 Dimethicone, Behentrimonium Chloride, PEG-200 Hydrogenated Glyceryl Palmate, PEG-7 Glyceryl Cocoate, Coco-Glucoside, Glyceryl Oleate, Dihydroxypropyl PEG-5 Linoleammonium Chlroide.

    Close
  • PRINCIPAL DISPLAY PANEL

    Clean Choice Foaming Alcohol Hand Sanitizer

    Certified Ecologo

    Certified NSF Instant Hand Antiseptic CCD-170

    USDA Certified Biobased Product

    1 Liter

    33.8 fl. oz.

    Part #0617381

    Distributed by Fastenal Co.

    Winona, MN 55987

    2013 fastenal.com

    Made in Canada

    0617381

    Alcohol Hand Sanitizer

    Rev. 08-13-116

    product label front

    product label back

    Close
  • INGREDIENTS AND APPEARANCE
    CLEAN CHOICE ALCOHOL SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11084-704
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Alcohol (Alcohol) Alcohol 70 L  in 100 L
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE  
    BEHENTRIMONIUM CHLORIDE  
    DIMETHICONE  
    COCO GLUCOSIDE  
    PEG-200 DILAURATE  
    GLYCERYL COCOATE  
    GLYCERYL MONOOLEATE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11084-704-27 1 L in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 09/15/2013
    Labeler - Deb USA, Inc. (607378015)
    Establishment
    Name Address ID/FEI Business Operations
    Deb Worldwide Healthcare Inc. 205662831 manufacture(11084-704)
    Close