DOCTRUST K- sodium flouride liquid

Doctrust K by

Drug Labeling and Warnings

Doctrust K by is a Otc medication manufactured, distributed, or labeled by Dr.s Medi Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

sodium fluoride

INACTIVE INGREDIENT

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

PURPOSE

Helps protect against cavities

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

- 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

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

dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DOCTRUST K 
sodium flouride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76670-0003
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	SODIUM FLUORIDE	0.74 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76670-0003-1	60 mL in 1 TUBE; Type 0: Not a Combination Product	08/22/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	08/22/2021

Labeler - Dr.s Medi Co.,Ltd. (694505169)

Registrant - Dr.s Medi Co.,Ltd. (694505169)

Establishment
Name	Address	ID/FEI	Business Operations
Dr.s Medi Co.,Ltd.		694505169	manufacture(76670-0003)