MIMIBO PREMIUM TOOTH- silicon dioxide, tocopherol acetate, tetrasodium pyrophosphate paste, dentifrice 
CONE MEDICAL 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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Silicon Dioxide

Tocopherol Acetate

Tetrasodium Pyrophosphate

D-Sorbitol Solution

Concentrated Glycerin

Carboxymethylcellulose Sodium

Hydroxyapatite

Medicinal Carbon

Chitosan

Mica

Zeolite

Bamboo Salt

Xylitol

Steviol Glycoside

Papain

Grapefruit Seed Extract

L-Menthol

Mentha Oil

Propolis Extract

Chamomile Extract
Rosemary Extract

Sage Extract

Aloe Extract

Glycyrrhiza Extract

Lavender Oil

Sodium Cocoyl Glutamate

Lauroyl Amidopropyl Dimethyl Glycine Solution

Deionized Water

For dental care

Keep out of reach of children

Apply an appropriate amount to your toothbrush and brush your teeth by brushing.

Warnings

Keep out of reach of children

■ If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Other Information

■ Store in an airtight container at room temperature

■ Date of use : 36 months from the date of manufacture

For dental use only

1

MIMIBO PREMIUM TOOTH 
silicon dioxide, tocopherol acetate, tetrasodium pyrophosphate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73527-0004
Route of AdministrationDENTAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE14 g  in 100 g
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE0.1 g  in 100 g
SODIUM PYROPHOSPHATE (UNII: O352864B8Z) (PYROPHOSPHORIC ACID - UNII:4E862E7GRQ) SODIUM PYROPHOSPHATE0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
XYLITOL (UNII: VCQ006KQ1E)  
LEVOMENTHOL (UNII: BZ1R15MTK7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73527-0004-120 g in 1 TUBE; Type 0: Not a Combination Product04/01/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/2021
Labeler - CONE MEDICAL Co., Ltd. (695811691)
Registrant - CONE MEDICAL Co., Ltd. (695811691)
Establishment
NameAddressID/FEIBusiness Operations
Sungwon Pharmaceutical689787898manufacture(73527-0004)
Establishment
NameAddressID/FEIBusiness Operations
CONE MEDICAL Co., Ltd.695811691manufacture(73527-0004)

Revised: 4/2021
Document Id: c1018820-6fae-6993-e053-2995a90a15eb
Set id: c101881a-5a12-2e04-e053-2a95a90a3f57
Version: 1
Effective Time: 20210428
 
CONE MEDICAL Co., Ltd.