MIMIBO PREMIUM TOOTH

Manufacturer: CONE MEDICAL Co., Ltd. | HealingStory.,LTD.
Effective date: 2025-01-02
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:50:35

Label at a glance#

ProductMIMIBO PREMIUM TOOTH

Active ingredientSILICON DIOXIDE, .ALPHA.-TOCOPHEROL ACETATE, SODIUM PYROPHOSPHATE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Silicon Dioxide

Tocopherol Acetate

Tetrasodium Pyrophosphate

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

For dental care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

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 SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73527-0003-1	2023-12-01	C162847	48780-1	0191ceaa-6c6f-198a-e063-dbdaa90aec3e	c0ff5df4-0b37-0b1b-e053-2a95a90a862c
73527-0003-1	2023-07-28	C162847	48780-1	0191ceaa-6c6f-198a-e063-dbdaa90aec3e	c0ff5df4-0b37-0b1b-e053-2a95a90a862c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73527-0003-1	MIMIBO PREMIUM TOOTH	100 g in 1 TUBE	PASTE, DENTIFRICE	100		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73527-0003	MIMIBO PREMIUM TOOTH (SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE) PASTE, DENTIFRICE [CONE MEDICAL CO., LTD.]	4	Current NDC, Legacy NDC, 1 package rows	20250104_c0ff5df4-0b37-0b1b-e053-2a95a90a862c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

MIMIBO PREMIUM TOOTH
Silicon Dioxide, Tocopherol Acetate, Tetrasodium Pyrophosphate
WATER
XYLITOL
LEVOMENTHOL
SILICON DIOXIDE
.ALPHA.-TOCOPHEROL ACETATE
.ALPHA.-TOCOPHEROL
SODIUM PYROPHOSPHATE
PYROPHOSPHORIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73527-0003	73527-0003-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
XYLITOL	VCQ006KQ1E	IACT
LEVOMENTHOL	BZ1R15MTK7	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	ACTIB
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	ACTIB
SODIUM PYROPHOSPHATE	O352864B8Z	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MIMIBO PREMIUM TOOTH	SILICON DIOXIDE, TOCOPHEROL ACETATE, TETRASODIUM PYROPHOSPHATE	CONE MEDICAL Co., Ltd.	c0ff5df4-0b37-0b1b-e053-2a95a90a862c	2025-01-02	Warnings	Exact identifier ndc (package): 73527-0003-1 ndc (product): 73527-0003 ndc11 (package): 73527000301 spl id: 2ac4fa58-43e0-e60c-e063-6394a90a3652 spl set id: c0ff5df4-0b37-0b1b-e053-2a95a90a862c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.