Denpo

Manufacturer
Suheung Capsule Co., Ltd
Effective date
2010-03-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:11

Label at a glance#

ProductDenpo cavity prevention
Active ingredientSODIUM FLUORIDE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient: Sodium Fluoride

DESCRIPTION SECTION

Benefits / Effects
(1) cavity prevention
(2) removal of bad breath, cleaning of oral cavity

Directions / dosage
(1) direction
take and chew one tablet, and clean teeth and gums using tongue and lips, rinse out with water
(2) dosage
2~5 times per day

Caution
(1) avoid direct sunlight, store in a cool dry place
(2) do not swallow

Warning
(1) the fluoride content of this product is 597.46 ppm (total fluoride content needs to be below 1,000 ppm)
(2) for children under six, use a pea-sized amount per use, do not eat or swallow
(3) immediately contact a physician if a child under six has swallowed a large portion
(4) keep and store away from children under six

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of box label
image of box label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313036sodium fluoride 1.1 MG Chewable TabletPSN1
313036sodium fluoride 1.1 MG Chewable TabletSCD1
313036sodium fluoride 1.1 MG (fluoride ion 0.5 MG) Chewable TabletSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52146-1001-12019-10-21C16284748780-1956f9ecf-c807-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52146-1001-1Denpocavity prevention60 in 1 PACKAGETABLET, CHEWABLE601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52146-1001DENPO CAVITY PREVENTION (FLUORIDE) TABLET, CHEWABLE [SUHEUNG CAPSULE CO., LTD]1Legacy NDC, 1 package rows20100407_54d94e7c-e62a-473f-b2fa-448396076dee.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W71
FLUORIDE IONACTIVE MOIETYQ80VPU408O1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52146-100152146-1001-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SODIUM FLUORIDE8ZYQ1474W7ACTIB

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
aab6ec68-7848-4a67-82dc-6f5b5636eb0f54d94e7c-e62a-473f-b2fa-448396076dee2010-03-18Exact identifier
spl id: aab6ec68-7848-4a67-82dc-6f5b5636eb0f
spl set id: 54d94e7c-e62a-473f-b2fa-448396076dee

Reported adverse events (FAERS/openFDA)#

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