Label: DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER ANTISEPTIC- alcohol aerosol, foam

  • NDC Code(s): 23667-104-00
  • Packager: Formulated Solutions, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 62% v/v

    Purpose

    Antiseptic

  • Uses(s)

    Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Extermely flammable, do not use near heat or flame or while smoking.

    Do not use

    • On children less than 2 months of age
    • On open skin wounds

    When using this product

    • keep out of eyes, ears, and mouth
    • In case of contact with eyes, rinse eyes thoroughly with water.
    • Do not puncture or incinerate
    • Contents under pressure
    • Do not expose to heat or store at temperature above 120°F (49°C)

    Stop use and ask a doctor

    • If irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children.

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

  • Directions

    • Hold can upside down and dispense into palm. Place enough product on hands to cover all surfaces. Rub hands together until dry
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

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

    Purified Water, Hydrofluorocarbon 152a; Isobutane; Emulsifying Wax NF; Propane

  • Package Labeling:

    Bottle2

  • INGREDIENTS AND APPEARANCE
    DOCTORS KLINE AND GREEN BOARD CERTIFIED DERMATOLOGIST HAND SANITIZER ANTISEPTIC 
    alcohol aerosol, foam
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:23667-104
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    ISOBUTANE (UNII: BXR49TP611)  
    PROPANE (UNII: T75W9911L6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:23667-104-00222 mL in 1 CAN; Type 0: Not a Combination Product02/09/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/09/2021
    Labeler - Formulated Solutions, LLC (143266687)
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