Label: DR. DADDYS GUMTOOTHPASTE- silicon dioxide, tetrasodium pyrophosphate, tocopherol acetate, sodium monofluorophosphate paste, dentifrice

  • NDC Code(s): 76884-0012-1
  • Packager: TB Healthcare Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

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 13, 2022

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  • ACTIVE INGREDIENT

    Silicon Dioxidel,Tetrasodium Pyrophosphate,Tocopherol Acetate,Sodium Monofluorophosphate

  • INACTIVE INGREDIENT

    D-Sorbitol Solution,Concentrated Glycerin,Xanthan gum,Sodium Cocoyl Glutamate,Ascorbic Acid,Hydroxyapatite,Xylitol,Sodium
    Chloride,Grapefruit Seed Extract,Glycyrrhiza Extract,Green Tea Extract,Matricaria Extract,Sage Extract,Aloe
    Extract,Eucalyptus Extract,Ginseng Extract,Propolis Extract,Ginger Powder,Myrrh Tincture,l-Menthol,Flavor,Water

  • PURPOSE

    Reduces bad breath, Prevents tartar buildup, Keeps mouth clean, Makes teeth white and strong, Prevent periodontal disease, gum disease

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • INDICATIONS & USAGE

    Put an appropriate amount on a toothbrush and brush teeth

  • WARNINGS

    1. Be careful not to swallow. Rinse mouth thoroughly after use

    2. If the use of toothpaste causes abnormalities such as gums or mouth injury, discontinue use and consult a doctor or dentist.

    3. For children under 6 years of age, use a small amount of toothpaste as small as pea per use, and use under the guidance of a guardian to avoid sucking or swallowing.

    4. If a child under 6 years old swallows large amount, consult with a doctor or dentist immediately.

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

  • DOSAGE & ADMINISTRATION

    For dental use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DR. DADDYS GUMTOOTHPASTE 
    silicon dioxide, tetrasodium pyrophosphate, tocopherol acetate, sodium monofluorophosphate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76884-0012
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE0.2 g  in 100 g
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE17 g  in 100 g
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z) (PYROPHOSPHORIC ACID - UNII:4E862E7GRQ) SODIUM PYROPHOSPHATE0.5 g  in 100 g
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.76 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    XYLITOL (UNII: VCQ006KQ1E)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76884-0012-1100 g in 1 TUBE; Type 0: Not a Combination Product04/13/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/06/2021
    Labeler - TB Healthcare Co., Ltd. (695035143)
    Registrant - TB Healthcare Co., Ltd. (695035143)
    Establishment
    NameAddressID/FEIBusiness Operations
    K.Boeun Pharmaceutical Co.,Ltd.695674074manufacture(76884-0012)