DOCTRUST 2X TOOTH- sodium fluoride paste 
DONG IL PHARMS CO.,LTD

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Sodium Flouride

Keep your teeth white and strong.
Keep your mouth clean.
Refresh the inside of the mouth.
Prevents tooth decay and bad breath by fluoride
Increase esthetic effect.
Removal of plaque (anti-plaque)
Prevention of gingivitis and periodontitis
Periodontal Disease Prevention
Prevention of gum disease

Keep out of reach of children

Brushing the teeth with a suitable amount

(1) Contains 1000ppm of fluoride.
(2) Do not swallow and rinse mouth thoroughly after use
(3) If you experience any problems with your gums or mouth during use,
discontinue use and consult your doctor.
(4) For children under 6 years of age, use small amounts of toothpaste. And
use itunder the supervision of a guardian to avoid sucking or swallowing.
(5) Consult a physician or dentist immediately if a child under 6 years old
hasswallowed large quantities.
(6) Keep out of the reach of children under 6 years of age.

Tocopherol Acetate, Silicon Dioxide, D-Sorbitol Solution, Carboxymethylcellulose Sodium, Chitosan, Propolis Extract, Glycyrrhiza Extract Powder, Ascorbic Acid, Green Tea Extract, Curcuma xanthorrhiza Extract, Xylitol, Enzymatically Modified Stevia, Sodium Cocoyl Glutamate, Sodium Bicarbonate, L-Menthol, Peppermint Oil, Water

For dental use only

label

DOCTRUST 2X TOOTH 
sodium fluoride paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73242-0100
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.22 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73242-0100-1100 g in 1 TUBE; Type 0: Not a Combination Product11/14/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35511/14/2019
Labeler - DONG IL PHARMS CO.,LTD (557810721)
Registrant - DONG IL PHARMS CO.,LTD (557810721)
Establishment
NameAddressID/FEIBusiness Operations
DONG IL PHARMS CO., LTD.557810721manufacture(73242-0100)

Revised: 11/2019
Document Id: 9747815e-3523-ce51-e053-2995a90a452d
Set id: 9747b758-a78d-faed-e053-2995a90a7012
Version: 1
Effective Time: 20191114
 
DONG IL PHARMS CO.,LTD