FDA.reportPublic FDA data

Dr.NOAH MARUFTOOTHPASTE

Manufacturer
DR.Noah | DONG IL PHARMS CO., LTD.
Effective date
2021-10-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:44:35

Label at a glance#

ProductDr.NOAH MARUFTOOTHPASTE
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure8 sections

Indications and uses

for oral use only

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Precipitated Calcium Carbonate
Xanthangum
Sodium Chloride
Steviol Glycoside
Xylitol
D-Sorbitol Solution
Concentrated Glycerin
Sodium Cocoyl Glutamate
Sodium Cocoyl Isethionate
Bioactive Herb Complex-C
L-Menthol
Menthol Pulegium Oil
Peppermint Oil
Spearmint Oil
Sage Extract
Aloe Extract
Green Tea Extract
Water

PURPOSE

OTC - PURPOSE SECTION

■ Keeps teeth white and strong

■ Keep the oral cavity clean

■ Prevents tooth decay and bad breath caused by fluoride

■ Removing plaque, preventing gingivitis and periodontitis

■ Periodontal Disease Prevention

■ Gum Disease Prevention

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNING

WARNINGS SECTION

For oral use only
When using this product

■ This toothpaste has a 1,000 ppm fluoride content

■ Do not use other than brushing teeth and be careful not to swallow

Keep out of reach of children

■ if swallowed, seek medical help or contact the poison control center immediately

USES

DOSAGE & ADMINISTRATION SECTION

for oral use only

INDICATION & USAGE SECTION

INDICATIONS & USAGE SECTION

Brush thoroughly ofter each meal or at least twice a day, as directed by yourdoctorordendst
Do not swallow.

Do not use if seal is broken or missing.

store in a cool, dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82359-0001-12023-01-30C16284748780-1f386c649-bc8f-0266-e053-dadaa90a7c1acf7bbc45-282c-7b02-e053-2995a90a2376

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82359-0001-1Dr.NOAH MARUFTOOTHPASTE120 g in 1 TUBEPASTE1201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82359-0001DR.NOAH MARUFTOOTHPASTE (SODIUM MONOFLUOROPHOSPHATE) PASTE [DR.NOAH]1Legacy NDC, 1 package rows20211030_cf7bbc45-282c-7b02-e053-2995a90a2376.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
82359-000182359-0001-1

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 CHLORIDE451W47IQ8XIACT
SORBITOL506T60A25RIACT
SODIUM MONOFLUOROPHOSPHATEC810JCZ56QACTIM

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
cf7bbc45-282a-7b02-e053-2995a90a2376cf7bbc45-282c-7b02-e053-2995a90a23762021-10-29WarningsExact identifier
spl id: cf7bbc45-282a-7b02-e053-2995a90a2376
spl set id: cf7bbc45-282c-7b02-e053-2995a90a2376

Reported adverse events (FAERS/openFDA)#

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