Label: LEMON LIME HAND SANITIZER SPRAY. 01- alcohol spray

  • NDC Code(s): 54860-427-01
  • Packager: Shenzhen Lantern Scicence Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 6, 2024

If you are a consumer or patient please visit this version.

  • Drug Facts
  • Active Ingredient

    Active ingredient Purpose

    Ethyl Alcohol 70% v/v Antiseptic

  • Uses

    Decreases bacieria on skin

  • Warning

    For external use only

  • When using this product

    Do not get into eyes. lf contact occurs, rinse thoroughly with water.

  • Do not use

    lf you are allergic to any of the ingredients

  • 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

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Gel, Aminomethy Propanol, Blue 1, Denatonium Benzoate, Fragrance, Glycerin, Tocopheryl Acetate, Water, Yellow 5.

  • 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
  • INGREDIENTS AND APPEARANCE
    LEMON LIME HAND SANITIZER SPRAY.  01
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-427
    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)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54860-427-0140 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/06/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/06/2024
    Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern Science Co.,Ltd.421222423manufacture(54860-427)