Label: CLOROX HAND SANITIZER- 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 April 21, 2021

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  • Active Ingredient

    Alcohol 71% v/v

  • Purpose

    Antiseptic

  • Use

    Hand sanitizer to help decrease bacteria on skin that can potentially cause disease.

  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.

    Do not use in the eyes.

    Discontinue use and ask a doctor if

    • irritation and redness develop.
    • condition persists for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

  • DIrections

    • Spray on clean, dry hands and nails
    • Wet hands thoroughly with product
    • Rub hands together for no less than 15 seconds, paying particular attention to interdigital spaces, fingernails and cuticles
    • Allow to dry without wiping
    • Rub hands together briskly until dry
  • Other Information

    • Store in a cool, dry place below 104 deg F (40 C)
  • Inactive Ingredients

    Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate

  • Questions or Comments?

    Visit us at www.brandbuzzcp.com or call us at: 1-888-508-4750.

  • PRINCIPAL DISPLAY PANEL

    Clorox

    Commercial

    Solutions

    CLOROX

    BLEACH-FREE

    Hand Sanitizer

    Kills greater than

    99.999%* of

    germs on contact

    Contains hand moisturizers

    Alcohol-based

    *of FDA organisms in the TFM for

    Topical Antimicrobial Drug

    Products

    16.9 FL OZ I 500 mL

    container label.jpg

  • INGREDIENTS AND APPEARANCE
    CLOROX HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0106
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERYL LAURATE (UNII: Y98611C087)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:26509-0106-159 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/06/2006
    2NDC:26509-0106-4500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/06/2006
    3NDC:26509-0106-51000 mL in 1 BOTTLE; Type 0: Not a Combination Product11/06/2006
    4NDC:26509-0106-61000 mL in 1 BAG; Type 0: Not a Combination Product11/06/2006
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/06/2006
    Labeler - The Clorox Company (009138033)
    Establishment
    NameAddressID/FEIBusiness Operations
    Best Sanitizers, Inc627278224manufacture(26509-0106)
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