FDA.reportPublic FDA data

DENTI BUONGIORNO PEACH MINT WHITENING TOOTH

Product NDC
85601-080
11-digit product format
856010080
Labeler code
85601
Product ID
85601-080_41194a31-0d8e-fd09-e063-6394a90a348c
Type
HUMAN OTC DRUG
Nonproprietary name
Hydrogen Peroxide, Silica
Dosage form
PASTE, DENTIFRICE
Route
ORAL
Labeler
ATOSAFE CO., Ltd
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-07-01
Substance
SILICON DIOXIDE; HYDROGEN PEROXIDE
Active strength
7; 2.14 g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
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 PEACH MINT WHITENING TOOTH
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILICON DIOXIDE7 g/100g
HYDROGEN PEROXIDE2.14 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
BBX060AN9VInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
41196c2f-8e2e-a54d-e063-6294a90ad8a7Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85601-080-01DENTI BUONGIORNO PEACH MINT WHITENING TOOTH100 g in 1 TUBEPASTE, DENTIFRICE1001
85601-080-02DENTI BUONGIORNO PEACH MINT WHITENING 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 PEACH MINT WHITENING TOOTHHYDROGEN PEROXIDE, SILICAATOSAFE CO., Ltd41196c2f-8e2e-a54d-e063-6294a90ad8a72025-10-14WarningsExact identifier
ndc (product): 85601-080

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85601-080-0185601008001100 g in 1 TUBE100 gHistorical
85601-080-02856010080021 TUBE in 1 CARTON (85601-080-02) / 100 g in 1 TUBE (85601-080-01) 1 tube2025-07-01NoNoCurrent