Label: LK HAND SANITIZER (ETHANOL)- 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 May 14, 2020

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  • Active ingredient

    Ethanol 70%

  • Uses

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

  • Purpose

    Antibacterial

  • Warnings

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

    Do not use

    • if you are allergic to any of the ingredients
    • in children less than 2 months of age
    • on open skin wounds

    When using this product avoid contact with eyes., ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    If pregnant or breast-feeding, ask a health professional before use.

  • Directions

    • Take appropriate amount onto your hand and spread it all the way to fingertips. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Inactive ingredients

  • Keep out of reach of children

  • LK Hand Sanitizer (Ethanol)

    lk hand sanitizer

  • INGREDIENTS AND APPEARANCE
    LK HAND SANITIZER (ETHANOL) 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74488-013
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74488-013-01500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/13/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/13/2020
    Labeler - Venice Cosmetic (695047082)
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