Label: LAFCO HAND SANITIZER BLUE MERCURY GRAPEFRUIT LAVENDER CUCUMBER- 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 April 20, 2023

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  • Drug Facts

  • Active ingredient

    Ethyl alcohol 73.2%

    Purpose

    Antiseptic

  • Use

    for hand washing to decrease bacteria on the skin

  • Warnings

    For external use only

    Flammable, keep away from fire or flame.

    Do not use

    in the eyes

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours

    Keep out of reach of children.

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

  • Directions

    wet hands thoroughly with product and allow to dry without wiping.

  • Other information

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

    Aqua(Water), Parfum(Fragrance), Glycerin, Aloe Barbadensis Leaf Juice, Acrylates/C10-30 AlkylAcrylateCrosspolymer, Triethanolamine, t-ButylAlcohol, PropyleneGlycol, Ethylene Brassylate, Citric Acid, Ginkgo Bioba Extract, Sodium Benzoate, Potassium Sorbate.

  • Package Labeling:380ml

    Bottle

  • Package Labeling:100ml

    Bottle2

  • INGREDIENTS AND APPEARANCE
    LAFCO HAND SANITIZER BLUE MERCURY GRAPEFRUIT LAVENDER CUCUMBER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77513-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL73.2 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GINKGO (UNII: 19FUJ2C58T)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77513-008-38380 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/202104/09/2024
    2NDC:77513-008-10100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/202112/03/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/01/202112/03/2024
    Labeler - GFL SA (486270809)
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