Doctrust K

Manufacturer: Dr.s Medi Co.,Ltd.
Effective date: 2021-08-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:42:03

Label at a glance#

ProductDoctrust K

Active ingredientSODIUM FLUORIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium fluoride

INACTIVE INGREDIENT SECTION

Hydroxyapatite, Curcuma extract, Xylitol, Centella asiatica extract, Houttuynia cordata extract, Green tea extract, Salvia officinalis extract, Eucalyptus globulus extract. Flavoring agent, Sodium cocoyl isethionate, Sodium cocoyl glutamate, Carboxymethylcellulose sodium, D-sorbitol solution, Enzymatically modified stevia, Purified water

OTC - PURPOSE SECTION

Helps protect against cavities

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

- Adults and children 2 years or older:

Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician

- Children 2 to 6 years

Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing).

- Children under 2 years of age:

Ask a dentist or physician.

WARNINGS SECTION

Keep out of reach of children under 6 years of age.
If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76670-0003-1	2022-07-29	C162847	48780-1	e4f33bdf-b356-d8a0-e053-dadaa90a6e4e	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76670-0003-1	Doctrust K	60 mL in 1 TUBE	LIQUID	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76670-0003	DOCTRUST K (SODIUM FLOURIDE) LIQUID [DR.S MEDI CO.,LTD.]	1	Legacy NDC, 1 package rows	20210824_ca19f21b-2b03-52b5-e053-2a95a90a0780.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Doctrust K
Sodium Flouride
WATER
SODIUM FLUORIDE
FLUORIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76670-0003	76670-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ca19d512-6b32-20c9-e053-2995a90aa004			ca19f21b-2b03-52b5-e053-2a95a90a0780	2021-08-21	Warnings	Exact identifier spl id: ca19d512-6b32-20c9-e053-2995a90aa004 spl set id: ca19f21b-2b03-52b5-e053-2a95a90a0780

Reported adverse events (FAERS/openFDA)#

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