Mint Dentistry

Manufacturer
Nutrix International, LLC. | Nutrix International, LLC
Effective date
2022-05-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:32

Label at a glance#

ProductMint Dentistry
Active ingredientSODIUM FLUORIDE
Label structure10 sections

Indications and uses

Aids in the prevention of dental decay.

Dosage and administration

Adults and children 2 years and over : Brush teeth thoroughly after each meal or at least twice a day, or as directed by a dentist or doctor. Children under 6 years of age : Use a pea-sized amount and supervise child's brushing and rinsing (to minimize swallowing). For children under 2 years of age : Ask a dentist or doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Sodium fluoride 0.24%

(0.15%w/v fluoride ion)

PURPOSE

OTC - PURPOSE SECTION

Anticavity

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Aids in the prevention of dental decay.

WARNING

WARNINGS SECTION

As with all fluoride toothpaste, keep out of reach of children under 6 years old. If you accidentally swallow more than used for brushing, get medical help or call a Poison Control Center right away.

KEEP OUT OF REACH SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age.

DIRECTIONS

INSTRUCTIONS FOR USE SECTION

Adults and children 2 years and over: Brush teeth thoroughly after each meal or at least twice a day, or as directed by a dentist or doctor.
Children under 6 years of age: Use a pea-sized amount and supervise child's brushing and rinsing (to minimize swallowing). For children under 2 years of age: Ask a dentist or doctor.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Inactive IngredientsInactive IngredientsGlycerin, Sorbitol, Hydrated Silicas, Water (Aqua), Xylitol, Cocamidopropyl Betaine, Mentha Viridis (Spearmint) Leaf Oil, Stevia Rebaudiana Leaf /Steam Extract, Xanthan Gum, Activated Charcoal.

QUESTIONS?

OTC - QUESTIONS SECTION

Call 833.879.6468

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Use a pea-sized amount via oral TubeTube

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front PackageFront Package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416783sodium fluoride 0.24 % ToothpastePSN2
416783sodium fluoride 0.0024 MG/MG ToothpasteSCD2
416783sodium fluoride 0.24 % (fluoride ion 0.13 % ) ToothpasteSY2
416783sodium fluoride 0.24 % (fluoride ion 0.14 % ) ToothpasteSY2
416783sodium fluoride 0.24 % (fluoride ion 0.15 % ) ToothpasteSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73333-115-01Mint Dentistry113 g in 1 TUBEPASTE1132

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73333-115MINT DENTISTRY (CHARCOAL SPEARMINT) PASTE [NUTRIX INTERNATIONAL, LLC.]2Legacy NDC, 1 package rows20220511_a382d2f5-be99-3bc5-e053-2995a90a1d19.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73333-11573333-115-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
deaed4ba-c866-9d99-e053-2a95a90a9317a382d2f5-be99-3bc5-e053-2995a90a1d192022-05-10WarningsExact identifier
spl id: deaed4ba-c866-9d99-e053-2a95a90a9317
spl set id: a382d2f5-be99-3bc5-e053-2995a90a1d19

Reported adverse events (FAERS/openFDA)#

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