Label: CLOROX CARE CONCEPTS 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 14, 2014

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  • Active ingredient

    Alcohol 67 percent

  • Purpose

    Antiseptic

  • Use

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

  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only.

  • WHEN USING

    When using this product, do not use in the eyes.

  • STOP USE

    Discontinue use and ask a doctor if

    • irritate and redness develop.
    • condition persists for more than 72 hours.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

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

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Other Information

    Store in a cool, dry place below 104 deg F (40 deg C).

  • Inactive ingredients

    Water, Isopropyl Alcohol, Glycerin, Glyceryl Laurate.

  • PRINCIPAL DISPLAY PANEL

    Hand Sanitizer Label

    Clorox Care Concepts

    Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    CLOROX CARE CONCEPTS HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL LAURATE (UNII: Y98611C087)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:26509-0002-159 mL in 1 BOTTLE, SPRAY
    2NDC:26509-0002-2236 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/07/2014
    Labeler - The Clorox Company (009138033)
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