Label: CLOROX CARE CONCEPTS- kit

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Exempt device

Drug Label Information

Updated August 21, 2014

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

  • Active Ingredient

    Alcohol 67%

  • 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

    HomeCareCleanUp

    Clorox Care Concepts

    Home Care Clean Up Kit

    Nitrile Non-Latex Exam Gloves

    Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    CLOROX CARE CONCEPTS 
    patient personal hygiene kit kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NHRIC:26509-0005
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NHRIC:26509-0005-11 in 1 KIT04/07/2014
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE, SPRAY 59 mL
    Part 20 PACKAGE
    Part 1 of 2
    CLOROX CARE CONCEPTS HAND SANITIZER 
    alcohol solution
    Product Information
    Item 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
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/07/2014
    Part 2 of 2
    NITRILE NON-LATEX GLOVES 
    patient examination glove
    Product Information
    Item Code (Source)GS1:8438995971
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    15 in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    premarket notificationK051378
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    exempt deviceABC04/07/2014
    Labeler - The Clorox Company (009138033)
    Registrant - The Clorox Company (009138033)