Label: ELLEN HAND SANITIZER2- ethyl alcohol spray

  • NDC Code(s): 85537-102-02
  • Packager: PT. SUPER HOME PRODUCT INDONESIA
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 21, 2025

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

  • USE

    Use Hand sanitizer to help reduce bacteria that potentially can cause diseaseFor use when soap and water are not ava'lable.

  • Warnings

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

  • Inactive ingredients

    Water,Fragrance, Aloe Extract,Glycerin, CarbomerTocopherylAcetate,Aminomethyl Propanol.

  • Directions

    • Place enough product on hands to cover all surfaces.Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoidswalowing.Not recommended for infants.
  • Keep out of reach of children.

    lf swallowed, get medical help or contact a PoisonControlCenter right away.

  • Purpose

    Antimicrobial,Hand Sanitizer

  • Active ingredient

    Ethyl alcohol 60%v/v Purpose:Antimicrobial

  • PRINCIPAL DISPLAY PANEL

    package label

  • INGREDIENTS AND APPEARANCE
    ELLEN HAND SANITIZER2 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85537-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.001 mL  in 100 mL
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.005 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 2 mL  in 100 mL
    CARBOMER (UNII: 0A5MM307FC) 0.01 mL  in 100 mL
    AQUA (UNII: 059QF0KO0R) 36.884 mL  in 100 mL
    ALOE (UNII: V5VD430YW9) 0.1 mL  in 100 mL
    FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) 1 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:85537-102-0245 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/21/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00504/21/2025
    Labeler - PT. SUPER HOME PRODUCT INDONESIA (564862692)
    Registrant - PT. SUPER HOME PRODUCT INDONESIA (564862692)
    Establishment
    NameAddressID/FEIBusiness Operations
    PT. SUPER HOME PRODUCT INDONESIA564862692manufacture(85537-102)