BON SCENT Sparkling Tooth Wash

Manufacturer
Lucella Co.,ltd | EQMAXON Corp.
Effective date
2019-04-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:59:14

Label at a glance#

ProductBON SCENT Sparkling Tooth Wash
Active ingredientSodium Fluoride
Label structure8 sections

Indications and uses

Uses: Helps protect against cavities

Dosage and administration

Directions: - Put 1 tablet into your mouth and wash your gums, teeth, and tongue using your tongue and lips. -Lastly rinse several times with water.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Sodium Fluoride 1.1%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:


DL-Malic acid, DL-Camphor, Glyceryl Monostearate, Glycyrrhizinic acid, Sodium Lauroyl Sarcosinate, Mannitol, Menthol, peppermint oil, Sodium Saccharin dihydrate, Magnesium stearate, Xylitol, Tricalcium phosphate, Calcium Carbonate, Colloid Silica, Sodium bicarbonate, PEG-150, Enzymatically Modified Stevia, Hydroxypropylmethylcellulose

PURPOSE

OTC - PURPOSE SECTION

Purpose: Anticaries & Anticavity

WARNINGS

WARNINGS SECTION

Warnings:


- Keep in a cool and dry place.
- Do not swallow.
- The fluorine content is 583.21ppm. (Total content should be less than 1,000ppm)
- If a child under 6 years of age swallowed large quantities, consult a physician or dentist immediately.
- Keep out of the reach of children under 6 years.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children under 6 years.

Uses

INDICATIONS & USAGE SECTION

Uses:
Helps protect against cavities

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:
- Put 1 tablet into your mouth and wash your gums, teeth, and tongue using your tongue and lips.
-Lastly rinse several times with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of pouchImage of pouch

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809115163684GTIN-13: 8809115163684
EAN-13: 8809115163684
GTIN storage (14 digits): 08809115163684
bon pouch.jpg
QR code linkQR Codem.site.naver.com/0gmBNbon pouch.jpg
QR code linkQR Codeuqr.kr/q.asp?idx=95dbon pouch.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72869-010-022021-01-29C16284748780-1ba0f9c33-4e1a-a910-e053-dadaa90a0b85a8a409c7-a3c2-49c0-91df-052f2a7a08b3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72869-010-01BON SCENT Sparkling Tooth Wash853 mg in 1 BLISTER PACKTABLET8532
72869-010-02BON SCENT Sparkling Tooth Wash30 in 1 POUCHTABLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72869-010BON SCENT SPARKLING TOOTH WASH (SODIUM FLUORIDE) TABLET [LUCELLA CO.,LTD]2Legacy NDC, 2 package rows20190417_a8a409c7-a3c2-49c0-91df-052f2a7a08b3.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72869-01072869-010-01, 72869-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Sodium Fluoride8ZYQ1474W7ACTIM
Mannitol3OWL53L36AIACT
MentholL7T10EIP3AIACT

Source Document#

Source XML · Source PDF

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
d95e5a00-3461-47a5-ab94-ae8f33864e65a8a409c7-a3c2-49c0-91df-052f2a7a08b32019-04-17WarningsExact identifier
spl id: d95e5a00-3461-47a5-ab94-ae8f33864e65
spl set id: a8a409c7-a3c2-49c0-91df-052f2a7a08b3

Reported adverse events (FAERS/openFDA)#

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