DOCTRUST DOUBLEX TOOTH- sodium fluoride paste, dentifrice

DOCTRUST DOUBLEX Tooth by

Drug Labeling and Warnings

DOCTRUST DOUBLEX Tooth by is a Otc medication manufactured, distributed, or labeled by Dr.s Medi Co.,Ltd., DONG IL PHARMS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Sodium fluoride 0.22%
(Total Fluoride Content 1,000 ppm Approx.)

INACTIVE INGREDIENTS

Sodium Tocopheryl Acetate, Silicon Dioxide, Chitosan, Propolis Extract, D-sorbitol Solution, Sodium Carboxymethyl Cellulose, Licorice Extract, Ascorbic Acid, Camellia Sinensis Extract, Curcumin Extract, Xylitol, Enzymatically Modified Stevia, Sodium Cocoylglutamate, Sodium Bicarbonate, L-menthol, Peppermint Oil, Purified Water

PURPOSE

Anticavity Toothpaste

WARNINGS

■ Do not swallow and rinse mouth thoroughly after use
■ 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

INGREDIENTS AND APPEARANCE

DOCTRUST DOUBLEX TOOTH 
sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76670-0010
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium fluoride (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.22 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
Silicon Dioxide (UNII: ETJ7Z6XBU4)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76670-0010-2	1 in 1 CARTON	10/01/2021
1	NDC: 76670-0010-1	100 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	10/01/2021

Labeler - DOCSMEDI OralBiome Co., Ltd. (694505169)

Registrant - DOCSMEDI OralBiome Co., Ltd. (694505169)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(76670-0010)