MEDIF WHITE TOOTH- hydrated silica, aluminium chlorohydrate, allantoinate 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.

----------

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

Image of carton

MEDIF WHITE TOOTH 
hydrated silica, aluminium chlorohydrate, allantoinate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72346-120
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDRATED SILICA (UNII: Y6O7T4G8P9) (HYDRATED SILICA - UNII:Y6O7T4G8P9) HYDRATED SILICA16.90 g  in 130 g
ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE0.65 g  in 130 g
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.65 g  in 130 g
Inactive Ingredients
Ingredient NameStrength
SORBITOL (UNII: 506T60A25R)  
Glycerin (UNII: PDC6A3C0OX)  
Xanthan gum (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72346-120-021 in 1 CARTON10/01/2020
1NDC:72346-120-01130 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other10/01/2020
Labeler - MEDIF CO.,LTD (694955391)
Registrant - MEDIF CO.,LTD (694955391)
Establishment
NameAddressID/FEIBusiness Operations
DONG IL PHARMS CO., LTD.557810721manufacture(72346-120)

Revised: 10/2020
Document Id: 4b01d8d9-7429-4981-93d7-38ead4d82135
Set id: fe1237e5-57cb-43b6-a9c6-cea550f2c87b
Version: 1
Effective Time: 20201027
 
MEDIF CO.,LTD