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NBF Gingival (NanoCureTech)

Available Formats

Dosage Form Package Information Links
GEL 30 g in 1 TUBE (23636-1001-1) Label Information

Complete NBF Gingival Information

  • ACTIVE INGREDIENT

    active ingredient: sodium monofluorophosphate

  • INACTIVE INGREDIENT

    inactive ingredient: silicon dioxide, triclosan, glycerin, d-sorbitol, polyethylene glycol, chitosan oligosaccharide, carboxymethylcellulose sodium, propolis extract, xylitol, sacccharin sodium hydroate, peppermint oil, l-menthol, sodium benzoate, ascorbic acid, tocopherol, purified water

  • PURPOSE

    â–  prevention of gingival disease

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    apply toothpast on soft bristle toothbrush and brush

  • WARNINGS

    if irritation occurs when using this product, discontinue use

  • DOSAGE & ADMINISTRATION

    â–  apply three times a day after meals

  • INGREDIENTS AND APPEARANCE
    NBF GINGIVAL 
    sodium monofluorophosphate gel
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:23636-1001
    Route of Administration DENTAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM MONOFLUOROPHOSPHATE 0.4 g  in 30 g
    Inactive Ingredients
    Ingredient Name Strength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBITOL (UNII: 506T60A25R)  
    CHITOSAN OLIGOSACCHARIDE (UNII: 23R93M6Y64)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
    XYLITOL (UNII: VCQ006KQ1E)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    MENTHA PIPERITA (UNII: 79M2M2UDA9)  
    MENTHOL (UNII: L7T10EIP3A)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:23636-1001-1 30 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 11/11/2011
    Labeler - NanoCureTech (557799555)
    Registrant - NanoCureTech (557799555)
    Establishment
    Name Address ID/FEI Business Operations
    Sungwon Pharmaceutical Co., Ltd 689787898 manufacture