Label: LEMYN ORGANICS MEDICAL-GRADE HAND SANITIZER- alcohol gel

  • NDC Code(s): 79835-701-02, 79835-701-08, 79835-701-12
  • Packager: Lemyn LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 16, 2024

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Uses

    Health care personnel + consumer grade 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
    • Flammable
    • Keep away from heat or flame

    When using this product

    keep out of 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 appears and lasts

    Keep out of reach of children.

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

    Do not use

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

    • Put enough product in your palm to cover hands. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product.
    • Avoid swallowing.
  • Inactive Ingredients

    Water (Aqua), Glycerin* (plant based), Aloe Barbadensis Leaf Extract*, Sodium Hyaluronate, Simmondsia Chinensis (Jojoba) Seed Oil*, Persea Gratissima (Avocado) Oil*, Helianthus Annuus (Sunflower) Seed Oil*, Panthenol, Tocopheryl Acetate, Citrus Sinensis (Orange) Fruit Extract, Carbomer, Aminomethyl Propanol

    *Organic

  • Other Information

    • Store below 104F (40C)
    • Avoid freezing and excessive heat above 104F (40C)
    • May discolor certain fabrics or sufaces.
  • Questions or comments?

    Call 877-262-1971

  • Company Information

    Distributed by Lemyn, LLC

    Santa Barbara, CA 93108

    Questions or comments?

    Visit lemyn.com

  • Product Packaging - 355 mL

    1

  • INGREDIENTS AND APPEARANCE
    LEMYN ORGANICS MEDICAL-GRADE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79835-701
    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
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    JOJOBA OIL (UNII: 724GKU717M)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ORANGE (UNII: 5EVU04N5QU)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    AVOCADO OIL (UNII: 6VNO72PFC1)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79835-701-12355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2020
    2NDC:79835-701-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2020
    3NDC:79835-701-0259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/06/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/06/2020
    Labeler - Lemyn LLC (064274271)
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