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

Dr.DADDYS Junior Toothpaste(Mint flavor) by

Drug Labeling and Warnings

Dr.DADDYS Junior Toothpaste(Mint flavor) 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

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

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76884-0007
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	15 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	0.758 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: 76884-0007-1	60 g in 1 TUBE; Type 0: Not a Combination Product	02/26/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		02/26/2022

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(76884-0007)