Label: CLOROX HEALTHCARE GBG ALOEGEL INSTANT HAND SANITIZER- alcohol liquid

  • 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 28, 2021

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  • Active ingredient

    Ethyl Alcohol 64% w/w

  • Purpose

    Antiseptic

  • Uses

    • for hand-washing to decrease bacteria on the skin when water is not available
  • Warnings

    FLAMMABLE. Keep away from fire or flame

    For external use only

  • WHEN USING

    When using this product

    • do not use in or near eyes
    • discontinue use if irritation andredness develop
    • do not use on deep or puncture woulds; consult your doctor
  • 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.

  • Directions

    • apply gel liberally to unsoiled hands and rub thoroughly
    • allow to dry without wiping or rinsing
  • Other information

    • store at room temperature
  • Inactive ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, D&C Yellow #10, FD&C Blue #1, FD&C Yellow #5, Fragrance, Glycereth-2 Cocoate, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Triethanolamine, Water

  • PRINCIPAL DISPLAY PANEL

    CLOROX

    HEALTHCARE

    GBG Aloe Gel

    Does Not Contain Bleach

    Formerly

    GBG AloeGel

    from HealthLink

    Instant Hand Sanitizer

    27 fl oz (800 mL)

    container label

  • INGREDIENTS AND APPEARANCE
    CLOROX HEALTHCARE GBG ALOEGEL INSTANT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:26509-0200
    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
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:26509-0200-2532 mL in 1 BOTTLE; Type 0: Not a Combination Product07/09/2019
    2NDC:26509-0200-3800 mL in 1 BAG; Type 0: Not a Combination Product07/09/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/09/2019
    Labeler - The Clorox Company (009138033)
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