Medi W Tooth by MEDIF CO.,LTD / DONG IL PHARMS CO.,LTD

Medi W Tooth by

Drug Labeling and Warnings

Medi W Tooth by is a Otc medication manufactured, distributed, or labeled by MEDIF CO.,LTD, DONG IL PHARMS CO.,LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

MEDI W TOOTH- hydrogen peroxide solution, colloidal silicon dioxide paste, dentifrice 
MEDIF CO.,LTD

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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ACTIVE INGREDIENTS

Hydrogen Peroxide Solution (35%) 2.14%
Colloidal Silicon Dioxide 7%

INACTIVE INGREDIENTS

Aqua, Concentrated Glycerin, Polyethylene Glycol 1500, Sodium Lauryl Sulfate, Xanthan gum, Carboxymethylcellulose Sodium, L-Menthol, Citrus Mint Flavor, Peppermint Oil, Enzymatically Modified Stevia, Xylitol, Green Tea Extract, Eucalyptus Extract, Taraxacum officinale Extract

PURPOSE

Whitening
Anti plaque

WARNINGS

Keep out of the 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.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children under 6 years of age.

Uses

■ Keep your tooth white and strong.
■ Keep your mouth clean.
■ Refresh inside of the mouth.
■ To prevent tooth decay and remove bad breath.
■ Increase esthetic effect.
■ Removal of plaque(anti-plaque).

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 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: Ask a dentist or physician

QUESTIONS

CONSUMER CONSULTING CENTER 070-4789-2000

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MEDI W TOOTH 
hydrogen peroxide solution, colloidal silicon dioxide paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72346-110
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V)	HYDROGEN PEROXIDE	2.35 g  in 110 g
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	7.7 g  in 110 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72346-110-02	1 in 1 CARTON	08/01/2020	08/30/2020
1	NDC: 72346-110-01	110 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
unapproved drug other		08/01/2020	08/30/2020

Labeler - MEDIF CO.,LTD (694955391)

Registrant - MEDIF CO.,LTD (694955391)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO.,LTD		557810721	manufacture(72346-110)

Revised: 3/2025

Document Id: 2ff7aa5a-ba47-c644-e063-6394a90a3d08

34390-5

Set id: e36ad94c-ed88-4142-af39-e6f948204abc

Version: 2

Effective Time: 20250310