DR. DADDYS GUMTOOTHPASTE- silicon dioxide, tetrasodium pyrophosphate, tocopherol acetate, sodium monofluorophosphate paste, dentifrice 
TB Healthcare Co., Ltd.

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.

----------

Silicon Dioxidel,Tetrasodium Pyrophosphate,Tocopherol Acetate,Sodium Monofluorophosphate

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

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

Put an appropriate amount on a toothbrush and brush teeth

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.

For dental use only

label

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)

Revised: 4/2022
Document Id: dc82bc61-67a2-3808-e053-2a95a90ae465
Set id: dc82bc1f-c32b-72c2-e053-2995a90a1072
Version: 1
Effective Time: 20220413
 
TB Healthcare Co., Ltd.