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

Dr. DADDYS GumToothpaste by

Drug Labeling and Warnings

Dr. DADDYS GumToothpaste by is a Otc medication manufactured, distributed, or labeled by TB Healthcare Co., Ltd., K.Boeun Pharmaceutical Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

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

Product 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)