Label: ATO TELL- menthol, garlic oil liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated April 6, 2023

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  • ACTIVE INGREDIENT

    menthol, garlic oil

  • PURPOSE

    digestion

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    shake the container for 2 to 3 times before use, apply it evenly

  • WARNINGS

    ■ if following abnormal symptoms occurs after use , stop use and consult with a skin specialist

    red specks, swelling, itching

    ■ don’t use on the part where there is injury, eczema, or dermatitis

    Keep out of reach of children

    ■ if swallowed, get medical help or contact a person control center immediately

  • INACTIVE INGREDIENT

    purified water
    Batylene Glycol
    allantoin
    SODIUMHYALURONATE
    Solubiliser
    1.2Hexanediol
    Vitamin E
    Carbomer
    DisodiumEDTA
    TEA TREE oil
    citrus junos seed oil
    Avandula Angustifolia(Lavander) oil

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ATO TELL 
    menthol, garlic oil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82994-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.2 g  in 100 mL
    GARLIC OIL (UNII: 4WG8U28833) (GARLIC OIL - UNII:4WG8U28833) GARLIC OIL7.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALLANTOIN (UNII: 344S277G0Z)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82994-0002-1100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/07/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/07/2023
    Labeler - sunkyung trading (695235330)
    Registrant - sunkyung trading (695235330)
    Establishment
    NameAddressID/FEIBusiness Operations
    sunkyung trading695235330manufacture(82994-0002)