MEDIF WHITE TOOTH- hydrated silica, aluminium chlorohydrate, allantoinate paste, dentifrice

MEDIF WHITE TOOTH by

Drug Labeling and Warnings

MEDIF WHITE 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]

ACTIVE INGREDIENTS

Hydrated Silica 14.0%
Aluminium Chlorohydrate, Allantoinate 0.5%

INACTIVE INGREDIENTS

D-Sorbitol Solution, Concentrated Glycerin, Xanthangum, Grapefruit Seed Extract, Matricaria Extract, Eucalyptus Extract, Propolis Extract, Glycyrrhiza Extract Powder, Bitter Orange peel Extract , Lettuce Extract(1) Active Carbon, Argentum, Hydroxy apatite, Xylitol, Enzymatically Modified Stevia, L-Menthol, Peppermint Oil, Anetol, Sodium Cocoyl Glutamate, Aqua)

PURPOSE

Anticavity

WARNINGS

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

KEEP OUT OF REACH OF CHILDREN

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

Uses

■ Keep it white and make it strong.
■ Keep the oral cavity clean.
■ Refreshes the oral cavity. effect.
■ Prevention of gingivitis and bad breath.
■ Increase the aesthetic
■ Prevent tooth decay and remove periodontitis(alveolar fistula)
■ Prevention ofperiodontal disease and gum disease
■ Plaque removal (antiplaque)

Directions

Put an appropriate amount on a toothb rush and brush your teeth by brushing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MEDIF WHITE TOOTH 
hydrated silica, aluminium chlorohydrate, allantoinate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72346-120
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDRATED SILICA (UNII: Y6O7T4G8P9) (HYDRATED SILICA - UNII:Y6O7T4G8P9)	HYDRATED SILICA	16.90 g  in 130 g
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M)	ALUMINUM CHLOROHYDRATE	0.65 g  in 130 g
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	0.65 g  in 130 g

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
Glycerin (UNII: PDC6A3C0OX)
Xanthan gum (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72346-120-02	1 in 1 CARTON	10/01/2020
1	NDC: 72346-120-01	130 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		10/01/2020

Labeler - MEDIF CO.,LTD (694955391)

Registrant - MEDIF CO.,LTD (694955391)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(72346-120)