Label: DR.DADDYS JUNIOR TOOTHPASTE(MINT FLAVOR)- tetrasodium pyrophosphate, sodium monofluorophosphate, dental type silica paste, dentifrice

  • NDC Code(s): 76884-0007-1
  • Packager: TB Healthcare Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated April 6, 2022

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  • ACTIVE INGREDIENT

    Sodium Monofluorophosphate, Dental type silica,
    Tetrasodium Pyrophosphate

  • INACTIVE INGREDIENT

    D-Sorbitol Solution
    Concentrated Glycerin
    Xanthangum
    Sodium Cocoyl Glutamate
    Ascorbic Acid
    Hydroxyapatite
    Xylitol
    Enzymatically Modified Stevia
    Sodium Chloride
    Flavor(Apple mint)
    Spearmint Oil
    Grapefruit Seed Extract
    Green Tea Extract
    Matricaria Extract
    Sage Extract
    Eucalyptus Extract
    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 JUNIOR TOOTHPASTE(MINT FLAVOR) 
    tetrasodium pyrophosphate, sodium monofluorophosphate, dental type silica paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76884-0007
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE15 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 ION0.758 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    XYLITOL (UNII: VCQ006KQ1E)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76884-0007-160 g in 1 TUBE; Type 0: Not a Combination Product02/26/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/26/2022
    Labeler - TB Healthcare Co., Ltd. (695035143)
    Registrant - TB Healthcare Co., Ltd. (695035143)
    Establishment
    NameAddressID/FEIBusiness Operations
    K.Boeun Pharmaceutical Co.,Ltd.695674074manufacture(76884-0007)
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