DOCTRUST 2X TOOTH

Manufacturer
DONG IL PHARMS CO.,LTD | DONG IL PHARMS CO., LTD.
Effective date
2019-11-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:01:22

Label at a glance#

ProductDOCTRUST 2X TOOTH
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Flouride

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

Brushing the teeth with a suitable amount

WARNINGS SECTION

(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.

INACTIVE INGREDIENT SECTION

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

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73242-010073242-0100-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
69a47b89-f022-4c6b-af0a-42d7bbc118099747b758-a78d-faed-e053-2995a90a70122021-11-05WarningsExact identifier
spl set id: 9747b758-a78d-faed-e053-2995a90a7012

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.