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
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Drug Label Information
Updated April 13, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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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
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. DADDYS GUMTOOTHPASTE
silicon dioxide, tetrasodium pyrophosphate, tocopherol acetate, sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76884-0012 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE 0.2 g in 100 g SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE 17 g in 100 g SODIUM PYROPHOSPHATE (UNII: O352864B8Z) (PYROPHOSPHORIC ACID - UNII:4E862E7GRQ) SODIUM PYROPHOSPHATE 0.5 g in 100 g SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 0.76 g in 100 g Inactive Ingredients Ingredient Name Strength XYLITOL (UNII: VCQ006KQ1E) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76884-0012-1 100 g in 1 TUBE; Type 0: Not a Combination Product 04/13/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/06/2021 Labeler - TB Healthcare Co., Ltd. (695035143) Registrant - TB Healthcare Co., Ltd. (695035143) Establishment Name Address ID/FEI Business Operations K.Boeun Pharmaceutical Co.,Ltd. 695674074 manufacture(76884-0012)