Label: LANISTY TOOTHPASTETABLETS tablet

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 6, 2024

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  • ACTIVE INGREDIENT

    Sodium Bicarbonate - (Baking Soda) 22%
    Menthol Formylethylamine - (Menthol) 9%
    Lactobacillus - (Lactobacillus) 1%

  • Purpose

    Keeps teeth white and strong.Keeps your mouth clean.Refreshes your mouth.Prevents tooth decay and elimina-tes bad breath.Enhances the aesthetic effectPrevention of gingivitis,periodontitis (pyorrhea alveolaris)Prevention of periodontal diseasePrevention of gum diseaseRemoval of plaque (Anti-plaque)

  • Uses

    Keeps teeth white and strong

  • Warnings

    Children need to be accompanied by a guadian

  • Do not use

    if this toothpaste causes anydamage to the gums or mouth,discontinue use and consultyour doctor or dentist.

  • When Using

    Avoid direct ingestion

  • Stop Use

    if this toothpaste causes anydamage to the gums or mouth,discontinue use and consultyour doctor or dentist.

  • Ask Doctor

    if a child under 6 years of ageswallows a large amount, imme-diately consult your doctor ordentist.

  • Keep Out Of Reach Of Children

    if swallowed, get medical help orcontact Poison Control Center right away.

  • INDICATIONS & USAGE

    1.Grab up a tablet and plance it your mouth
    2.Chew your tablet until fully dissolvrf.
    3.Brush with a wet toothbrushfor two minutes twice a day

  • Other information

  • INACTIVE INGREDIENT

    Maltodextrin
    Sodium Carbonate
    Light Calcium Carbonate
    Essence
    Sodium Lauryl Sulfate
    Xanthan Gum
    Trichlorogalactose
    Bioactive Glass
    Cocos Nucifera Shell Powder

  • Questions

    Email: commet515@gmail.com

  • DOSAGE & ADMINISTRATION

    Place tablets in your mouth.
    Chew until it foams.
    Brush your teeth as usual. Use twice daily.

  • PRINCIPAL DISPLAY PANEL

    toothpaste

  • INGREDIENTS AND APPEARANCE
    LANISTY TOOTHPASTETABLETS 
    lanisty toothpastetablets tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84766-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE22 g  in 100 g
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL9 g  in 100 g
    LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5) (LACTOBACILLUS ACIDOPHILUS - UNII:1PRR1V42V5) LACTOBACILLUS ACIDOPHILUS1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 1 g  in 100 g
    CALCIUM CARBONATE (UNII: H0G9379FGK) 13 g  in 100 g
    XANTHAN GUM (UNII: TTV12P4NEE) 3 g  in 100 g
    EPIRUBICIN HYDROCHLORIDE (UNII: 22966TX7J5) 17 g  in 100 g
    DIHYDROXYALUMINUM SODIUM CARBONATE (UNII: 84H8Z9550J) 15 g  in 100 g
    VANILLA (UNII: Q74T35078H) 10 g  in 100 g
    MALTODEXTRIN (UNII: 7CVR7L4A2D) 17 g  in 100 g
    SUCRALOSE (UNII: 96K6UQ3ZD4) 2 g  in 100 g
    SODIUM LAURYL SULFATE (UNII: 368GB5141J) 6 g  in 100 g
    COCONUT SHELL (UNII: 7O4218UHJ4) 1 g  in 100 g
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize6mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84766-0001-250 g in 1 BOTTLE; Type 0: Not a Combination Product09/23/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02209/23/2024
    Labeler - COMFMET LIMITED (989085771)
    Registrant - COMFMET LIMITED (989085771)
    Establishment
    NameAddressID/FEIBusiness Operations
    COMFMET LIMITED989085771manufacture(84766-0001)
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