Label: MEDIF WHITE TOOTH- hydrated silica, aluminium chlorohydrate, allantoinate paste, dentifrice

  • NDC Code(s): 72346-120-01, 72346-120-02
  • Packager: MEDIF CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 27, 2020

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  • ACTIVE INGREDIENTS

    Hydrated Silica 14.0%
    Aluminium Chlorohydrate, Allantoinate 0.5%

  • INACTIVE INGREDIENTS

    D-Sorbitol Solution, Concentrated Glycerin, Xanthangum, Grapefruit Seed Extract, Matricaria Extract, Eucalyptus Extract, Propolis Extract, Glycyrrhiza Extract Powder, Bitter Orange peel Extract , Lettuce Extract(1) Active Carbon, Argentum, Hydroxy apatite, Xylitol, Enzymatically Modified Stevia, L-Menthol, Peppermint Oil, Anetol, Sodium Cocoyl Glutamate, Aqua)

  • PURPOSE

    Anticavity

  • WARNINGS

    Keep out of the rech of children under 6 years of age.
    If more than used for brushing is accidentally swllowed, get medical help or contact a Poison Contol Center right away.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children under 6 years of age.

  • Uses

    ■ Keep it white and make it strong.
    ■ Keep the oral cavity clean.
    ■ Refreshes the oral cavity. effect.
    ■ Prevention of gingivitis and bad breath.
    ■ Increase the aesthetic
    ■ Prevent tooth decay and remove periodontitis(alveolar fistula)
    ■ Prevention ofperiodontal disease and gum disease
    ■ Plaque removal (antiplaque)

  • Directions

    Put an appropriate amount on a toothb rush and brush your teeth by brushing.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    MEDIF WHITE TOOTH 
    hydrated silica, aluminium chlorohydrate, allantoinate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72346-120
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYDRATED SILICA (UNII: Y6O7T4G8P9) (HYDRATED SILICA - UNII:Y6O7T4G8P9) HYDRATED SILICA16.90 g  in 130 g
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE0.65 g  in 130 g
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.65 g  in 130 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Xanthan gum (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72346-120-021 in 1 CARTON10/01/2020
    1NDC:72346-120-01130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2020
    Labeler - MEDIF CO.,LTD (694955391)
    Registrant - MEDIF CO.,LTD (694955391)
    Establishment
    NameAddressID/FEIBusiness Operations
    DONG IL PHARMS CO., LTD.557810721manufacture(72346-120)
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