DOCTRUST K TOOTH- silicon dioxide, sodium monofluorophosphate gel, dentifrice 
DOCSMEDI OralBiome 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.

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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

■ When using this product, if irritation occurs discontinue use, Stop use and ask a dentist if
■ For children under 6 years of age, use small amounts of toothpaste.
under the supervision of a guardian to avoid sucking or swallowing.
■ Consult a physician or dentist immediately if a child under 6 years old has swallowed large quantities.
■ Keep out of the 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: 82-43-883-2844

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton
DOCTRUST K TOOTH 
silicon dioxide, sodium monofluorophosphate gel, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76670-0014
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Silicon dioxide (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) Silicon dioxide16.0 g  in 100 g
Sodium monofluorophosphate (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.74 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)  
SORBITOL (UNII: 506T60A25R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76670-0014-21 in 1 CARTON12/01/2022
1NDC:76670-0014-160 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/01/2022
Labeler - DOCSMEDI OralBiome Co., Ltd. (694505169)
Registrant - DOCSMEDI OralBiome Co., Ltd. (694505169)
Establishment
NameAddressID/FEIBusiness Operations
DONG IL PHARMS CO., LTD.557810721manufacture(76670-0014)

Revised: 12/2023
Document Id: 90ad77d8-c0d4-4649-92b9-41ebb6ec561d
Set id: a02f8865-e7be-4ef4-b09c-dad846639764
Version: 2
Effective Time: 20231205
 
DOCSMEDI OralBiome Co., Ltd.