Label: CLOROX ANTIMICROBIAL HAND SANITIZER- ethyl alcohol gel

  • 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 January 25, 2016

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  • ACTIVE INGREDIENT

    Ethyl Alcohol 62% w/w

  • PURPOSE

    Antimicrobial

  • INDICATIONS & USAGE

    Uses

    • To sanitize hands without requiring water or a rinse

  • WARNINGS

    Warnings

    FLAMMABLE

    For external use only

  • WHEN USING

    When using this product

    • do not use near heat or flame

    • do not use in or near eyes

    • discontinue use if irritation and redness develop, or if condition persists for more than 72 hours

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • DOSAGE & ADMINISTRATION

    Directions

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

  • OTHER SAFETY INFORMATION

    Other Information

    • Store at room temperature

  • INACTIVE INGREDIENT

    Inactive ingredients

    • Aloe Barbadensis Leaf Juice
    • Carbomer
    • Diisopropylamine
    • FD&C Blue #1
    • Fragrance
    • Glycerin
    • Isopropyl Myristate
    • Phenoxyethanol
    • Tocopherol Acetate
    • Water
  • QUESTIONS

    QUESTIONS OR COMMENTS?

    Call 1-800-638-2625 or visit www.hlk.cc

  • PRINCIPAL DISPLAY PANEL

    Clorox Antimicrobial Hand Sanitizer

    18 FL OZ (532 mL) CLX Blue Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    CLOROX ANTIMICROBIAL HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:26509-0010-8532 mL in 1 BOTTLE; Type 0: Not a Combination Product01/25/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/25/2016
    Labeler - The Clorox Company (009138033)
    Registrant - Carroll Company (007372329)
    Establishment
    NameAddressID/FEIBusiness Operations
    Carroll Company007372329manufacture(26509-0010)
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