Label: CLOROX HAND SANITIZER- alcohol gel

  • NDC Code(s): 69540-0025-1, 69540-0025-2, 69540-0025-3, 69540-0025-4
  • Packager: Brand Buzz LLC
  • 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 February 2, 2023

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 71% v/v

    Purpose

    Antiseptic

  • Use

    Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

  • Warnings

    For external use only. Flammable. Keep away from fire or flame.

    When using this product

    do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    Discontinue use

    if irritation and redness develop. If condition persists for more than 72 hours consult a physician.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    • Squeeze gel into your palm and briskly rub hands together until dry.
    • Children under 6 years of age should be supervised when in use.
  • Other information

    • Store between 15 and 30C (59 and 86F).
    • Avoid freezing and excessive heat above 40C (104F).
  • Inactive ingredients

    Aloe Barbadensis Leaf Extract, Carbomer, Glycerin, Tocopheryl Acetate (Vitamin E), Triethanolamine, Water (Aqua).

  • Package Labeling:2ml

    LabelBox

  • Package Labeling:500ml

    Label2

  • Package Labeling:1000ml

    Label4

  • Package Labeling:1000ml Refill

    Bottle

  • INGREDIENTS AND APPEARANCE
    CLOROX HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69540-0025
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69540-0025-1100 in 1 BOX03/19/2021
    12 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:69540-0025-2500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/19/2021
    3NDC:69540-0025-31000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/19/2021
    4NDC:69540-0025-41000 mL in 1 BOTTLE; Type 0: Not a Combination Product03/19/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/19/2021
    Labeler - Brand Buzz LLC (079266204)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern Science Co. Ltd.421222423manufacture(69540-0025)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Guoyao Jingyue Aerosol Co., Ltd.554529812manufacture(69540-0025)
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