MIMIBO PREMIUM TOOTH- silicon dioxide, tocopherol acetate, tetrasodium pyrophosphate paste, dentifrice

MIMIBO PREMIUM TOOTH by

Drug Labeling and Warnings

MIMIBO PREMIUM TOOTH by is a Otc medication manufactured, distributed, or labeled by CONE MEDICAL Co., Ltd., Sungwon Pharmaceutical. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Silicon Dioxide

Tocopherol Acetate

Tetrasodium Pyrophosphate

INACTIVE INGREDIENT

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

PURPOSE

For dental care

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

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

WARNINGS

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

DOSAGE & ADMINISTRATION

For dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MIMIBO PREMIUM TOOTH 
silicon dioxide, tocopherol acetate, tetrasodium pyrophosphate paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73527-0004
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	14 g  in 100 g
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1)	.ALPHA.-TOCOPHEROL ACETATE	0.1 g  in 100 g
SODIUM PYROPHOSPHATE (UNII: O352864B8Z) (PYROPHOSPHORIC ACID - UNII:4E862E7GRQ)	SODIUM PYROPHOSPHATE	0.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
XYLITOL (UNII: VCQ006KQ1E)
LEVOMENTHOL (UNII: BZ1R15MTK7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73527-0004-1	20 g in 1 TUBE; Type 0: Not a Combination Product	04/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2021

Labeler - CONE MEDICAL Co., Ltd. (695811691)

Registrant - CONE MEDICAL Co., Ltd. (695811691)

Establishment
Name	Address	ID/FEI	Business Operations
HealingStory.,LTD.		688403124	manufacture(73527-0004)

Establishment
Name	Address	ID/FEI	Business Operations
CONE MEDICAL Co., Ltd.		695811691	label(73527-0004)