DOCTRUST K TOOTH- silicon dioxide, sodium monofluorophosphate gel, dentifrice

DOCTRUST K Tooth by

Drug Labeling and Warnings

DOCTRUST K Tooth by is a Otc medication manufactured, distributed, or labeled by DOCSMEDI OralBiome Co., Ltd., DONG IL PHARMS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Silicon dioxide 16.0%
Sodium monofluorophosphate 0.740%
(Total Fluoride Content 977 ppm Approx.)

Inactive ingredients

Carboxymethyl cellulose, D-sorbitol solution, Sodium Hydrogencarbonate, Enzymatically modified stevia, Xylitol, Hydroxyapatite, Turmeric root extract, Centellaasiatica extract, HouttuyniacordataThunberg extract, Green tea extract, Salvia officinalis(sage) extract, Eucalyptus extract, naturalaromatics(Lime, Green grape) Sodium cocoyl glutamate, Purified water

PURPOSE

Anticavity Toothpaste

WARNINGS

■ Do not swallow. Rinse mouth thoroughly after use.

■ For children under 6 years of age, use only a pea-sized amount of toothpaste under the supervision of a guardian to avoid sucking or swallowing.

■ If a child under 6 years of age swallows a large amount of toothpaste, consult a physician or dentist immediately.

■ Keep out of reach of children under 6 years of age.

KEEP OUT OF REACH OF CHILDREN

■ Keep out of the reach of children under 6 years of age.

Uses

■ Helps protect against cavities

Directions

■ Adults and children 2 years of age and older: Brush teeth thoroughly preferably after each meal or at least twice a day or as directed by a dentist or doctor.
■ Children under 6 years: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.
■ Children under 2 years: Consult a dentist or doctor.

Other Information

■ Do not store this product in an inappropriate place such as high or low temperatures or under direct sun light

Questions

■ https://docsmedi.kr

■ Tel: 82-031-922-2240, Fax: 82-031-365-4596

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DOCTRUST K TOOTH 
silicon dioxide, sodium monofluorophosphate gel, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76670-0014
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	16 g  in 100 g
SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.74 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
SORBITOL (UNII: 506T60A25R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76670-0014-2	1 in 1 CARTON	12/01/2022
1	NDC: 76670-0014-1	60 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/01/2022

Labeler - DOCSMEDI Co., Ltd. (694505169)

Registrant - DOCSMEDI Co., Ltd. (694505169)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(76670-0014)