FDA.reportPublic FDA data

DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH

Product NDC
85601-110
11-digit product format
856010110
Labeler code
85601
Product ID
85601-110_487d507d-0286-0753-e063-6294a90aadde
Type
HUMAN OTC DRUG
Nonproprietary name
Silica, Sodium Monofluorophosphate
Dosage form
PASTE, DENTIFRICE
Route
ORAL
Labeler
ATOSAFE CO., Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2026-01-02
Substance
SILICON DIOXIDE; SODIUM MONOFLUOROPHOSPHATE
Active strength
18; .76 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILICON DIOXIDE18 g/100g
SODIUM MONOFLUOROPHOSPHATE.76 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
ETJ7Z6XBU4Internal UNII lookup
C810JCZ56QInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2732211Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
487d52d1-8853-bc90-e063-6394a90ab91dAvailable on FDA.report

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

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 (product): 85601-110

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2732211silicon dioxide 18 % / sodium monofluorophosphate 0.76 % ToothpastePSN487d52d1-8853-bc90-e063-6394a90ab91d1
2732211silicon dioxide 0.18 MG/MG / sodium monofluorophosphate 0.0076 MG/MG ToothpasteSCD487d52d1-8853-bc90-e063-6394a90ab91d1
2732211silicon dioxide 18 % / sodium monofluorophosphate 0.76 % ToothpasteSY487d52d1-8853-bc90-e063-6394a90ab91d1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85601-110-0185601011001100 g in 1 TUBE100 gHistorical
85601-110-02856010110021 TUBE in 1 CARTON (85601-110-02) / 100 g in 1 TUBE (85601-110-01) 1 tube2026-01-02NoNoCurrent