Label: LARTT MOUTHWASH- sodium fluoride liquid

  • NDC Code(s): 61284-0014-1, 61284-0014-2
  • Packager: ECOWORLDPHARM CO.,LTD
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated April 5, 2024

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  • ACTIVE INGREDIENT

    sodium fluoride

  • INACTIVE INGREDIENT

    Glycerin, Xylitol, DL-Alanine, Stevia, Sea Salt, Green tea Extract., Chitosan, Ginger tincture, Licorice Extract, Panax Ginseng Root Extract, Centella Extract, Acetic acid, Sodium citrate, Citric Acid, Tea Tree Oil, Peppermint Oil, Eucalyptol, Shine Muscat Flavor Sorbic acid, Sodium carboxymethylcellulose, L-menthol, Purified water

  • PURPOSE

    Anticavity

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    Adult and over 12 years old

    ¡ Use twice a day after brushing your teeth with a toothpaste

    ¡ 30 seconds vigorously swish contents of one packet and spit out

    ¡ Do not swallow after rinsed

    ¡ Recommend do not eat or drink for 30 minutes after rinsed. It will be better results

    ¡ Supervise children as necessary until capable of suing withour supervision

    ¡ Consult with doctor or dentist before use if you have any injuries such as dental works in your mouth

  • WARNINGS

    if more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away

  • DOSAGE & ADMINISTRATION

    for dental use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    LARTT MOUTHWASH 
    sodium fluoride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61284-0014
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.05 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    XYLITOL (UNII: VCQ006KQ1E)  
    PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61284-0014-230 in 1 PACKAGE10/05/2023
    1NDC:61284-0014-113 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02110/05/2023
    Labeler - ECOWORLDPHARM CO.,LTD (688735061)
    Registrant - ECOWORLDPHARM CO.,LTD (688735061)
    Establishment
    NameAddressID/FEIBusiness Operations
    ECOWORLDPHARM CO.,LTD688735061manufacture(61284-0014)
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