DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH

Manufacturer
ATOSAFE CO., Ltd | DONG IL PHARMS CO., LTD.
Effective date
2026-01-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:33:31

Label at a glance#

ProductDENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH
Active ingredientSILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient(s)

Silica 18.0%

Sodium Monofluorophosphate 0.76%

OTC - PURPOSE SECTION

Purpose

Antiplaque, Anticavity

WARNINGS SECTION

Warnings

• Keep out of reach of children under 6 years of age.
• If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenunder 6 years of age.

INDICATIONS & USAGE SECTION

Use(s)

• Helps remove plaque and tartar buildup
• Helps prevent cavities
• Helps reduce gum inflammation and promote healthy teeth

DOSAGE & ADMINISTRATION SECTION

Directions

• Adults and children 2 years of age and older : Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician

• Children 2 to 6 years : Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)

• Children under 2 years : Ask a dentist or physician

OTHER SAFETY INFORMATION

Other Information

• Store at temperatures between 1°C and 30°C
• Use within 36 months from the date of manufacture
• Do not store in high/low temperatures or direct sunlight

OTC - QUESTIONS SECTION

Questions

+82-1588-9709

INACTIVE INGREDIENT SECTION

Inactive ingredients

D-Sorbitol Solution, Water(Aqua) ,Silicon Dioxide , Concentrated Glycerin, Sodium Cocoyl Glutamate, Polyethylene Glycol 1500, Carboxymethylcellulose Sodium, Sodium Monofluorophosphate, Sodium Bicarbonate, Titanium Oxide, Xylitol, Enzymatically Modified Stevia, Propolis Extract, Grapefruit Seed Extract, Aloe Extract, Matricaria Extract, Eucalyptus Extract, Sage Extract, Green Tea Extract, Rosemary Extract, Calendula Extract, Leontopodium Alpinum Extract, Curcuma Longa (Turmeric), Centella Extract, Houttuynia Cordata Extract, L-Menthol, Menthol Pulegium Oil, Herb Mint Flavor, Mild Mint Flavor, Sodium Lauroyl Sarcosinate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton ImageCarton Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2732211silicon dioxide 18 % / sodium monofluorophosphate 0.76 % ToothpastePSN1
2732211silicon dioxide 0.18 MG/MG / sodium monofluorophosphate 0.0076 MG/MG ToothpasteSCD1
2732211silicon dioxide 18 % / sodium monofluorophosphate 0.76 % ToothpasteSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85601-110-01DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH100 g in 1 TUBEPASTE, DENTIFRICE1001
85601-110-02DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH1 in 1 CARTONPASTE, DENTIFRICE11

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85601-11085601-110-01, 85601-110-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTHSILICA, SODIUM MONOFLUOROPHOSPHATEATOSAFE CO., Ltd487d52d1-8853-bc90-e063-6394a90ab91d2026-01-16WarningsExact identifier
ndc (package): 85601-110-02
ndc (package): 85601-110-01
ndc (product): 85601-110
ndc11 (package): 85601011001
ndc11 (package): 85601011002
spl id: 487d507d-0286-0753-e063-6294a90aadde
spl set id: 487d52d1-8853-bc90-e063-6394a90ab91d

Reported adverse events (FAERS/openFDA)#

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