Label: ASSORTED LICENSED HAND SANITIZER GRAPE 01- alcohol spray

  • NDC Code(s): 54860-423-01
  • Packager: Shenzhen Lantern Scicence Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 9, 2024

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  • Drug Facts

    drug factsDrug Facts

  • Active Ingredient

    Active ingredient Purpose

    Ethyl Alcohol 70% v/v Antiseptic

  • Uses

    Decreases bacieria on skin

  • Warning

    For external use only

  • Do not use

    lf you are allergic to any of the ingredients

  • When using this product

    Do not get into eyes. lf contact occurs, rinse thoroughly with water.Do not use in or near eyes,In case of eye contact ,flush eyes thoroughly with water. Discontinue if skin becomes irritated and ask for a doctor.

  • Stop use and ask a doctor

    lf irritation or rash develops and continues for more than72 hours.

  • keep out of reach of children

    lf swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    Adults and children 6 years and older
    Spray onto hands and rub together unil dry. Recommended for repeat use.
    Children under 6 years of age
    should be supervised when using this product.

  • Inactive ingredients

    Water, Fragrance,Glycerin, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, Aminomethyl Propanol, Tocopheryl Acetate, Aloe Barbadensis Gel, Denatonium Benzoate.

  • other Information


    Storebetween15-30C(59-86F)
    Avoid freezing and excessive heat above 40C (104F)

  • DOSAGE & ADMINISTRATION

    Spray 3-4 times each time.
    Used in the skin area of the hands.

  • packing

    packingpacking

  • INGREDIENTS AND APPEARANCE
    ASSORTED LICENSED HAND SANITIZER GRAPE  01
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-423
    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
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54860-423-0128 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product07/06/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/06/2024
    Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern Science Co.,Ltd.421222423manufacture(54860-423)
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