FDA.reportPublic FDA data

Doctor 9020 Dental Clinic

Manufacturer
JANGIN PHARM CO.,LTD.
Effective date
2019-12-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:02:01

Label at a glance#

ProductDoctor 9020 Dental Clinic
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient : Sodium fluoride

INACTIVE INGREDIENT SECTION

Preservatives-Sodium Benzoate

Other additives-L-Menthol, SophoraAngustifolia Root Extract, GlycyrrhizaInflata Root Extract, Glycerin, Camellia SinensisCatechins, Saccharin Sodium Hydrate, Sodium Citrate Hydrate, Citric Acid Hydrate, Xylitol, DI-Water, Caramel Colorant, Red Ginseng Extract, Polyoxyl 40 Hydrogenated Castor Oil

OTC - PURPOSE SECTION

Effect :prevent cavities, and remove bad breath

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

Administration and doses : Once a day (mainly before bed), use it after brushing thoroughly. 6 years old to adults:10ml into your mouth, mix well for 1 minute, then spit. Be careful not to eat or drink food for 30 minutes after use to obtain sufficient effect

WARNINGS SECTION

●Caution :1) The fluoride content of this product is 90.5ppm. 2) Do not use this product - Anyone who is hypersensitive to this product. 3) Other Precautions when using this product-Do not swallow. Do not use for children under 6 years old unless instructed by a dentist. Keep out of reach of children. If they drink lots of medicine, feed large amounts of milk and follow doctor's instructions. 4) Storage precautions and other precautions when using this product-Keep out of the reach of children. Avoid direct sunlight. To shade the light, store in a cool place. To prevent misuse and preserve quality, do not change the container

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69255-500-022021-01-29C16284748780-1ba0f9c33-20a5-a910-e053-dadaa90a0b8599ca7d9b-44c0-b1ac-e053-2995a90aecd8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69255-500-01Doctor 9020 Dental Clinic12 mL in 1 POUCHLIQUID121
69255-500-02Doctor 9020 Dental Clinic15 in 1 PACKAGELIQUID151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69255-500DOCTOR 9020 DENTAL CLINIC (SODIUM FLUORIDE) LIQUID [JANGIN PHARM CO.,LTD.]1Legacy NDC, 2 package rows20191216_99ca7d9b-44c0-b1ac-e053-2995a90aecd8.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
69255-50069255-500-01, 69255-500-02

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
XYLITOLVCQ006KQ1EIACT
LEVOMENTHOLBZ1R15MTK7IACT
SODIUM FLUORIDE8ZYQ1474W7ACTIM

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
99ca624d-733d-59fa-e053-2a95a90a5c9299ca7d9b-44c0-b1ac-e053-2995a90aecd82019-12-15WarningsExact identifier
spl id: 99ca624d-733d-59fa-e053-2a95a90a5c92
spl set id: 99ca7d9b-44c0-b1ac-e053-2995a90aecd8

Reported adverse events (FAERS/openFDA)#

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