3SECONDS MAGIC GARGLE PEACH

Manufacturer
SUNJINBIO CO.,LTD
Effective date
2020-02-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:03:40

Label at a glance#

Product3SECONDS MAGIC GARGLE PEACH
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Flouride

OTC - PURPOSE SECTION

For dental care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

1. Put one tablet in mouth.

2. Chew it.

3. Gargle for 30 sec.

4. Spit it out.

5. Rinse with water.

WARNINGS SECTION

1. The fluoride concentration of this toothpaste is 583.21 ppm.

2. Be careful not to swallow it, and rinse your mouth thoroughly after use.

3. If a child under 6 years of age swallows a large amount, consult a doctor or dentist immediately.

4. Keep out of reach of children under 6 years old.

INACTIVE INGREDIENT SECTION

MALIC ACID, HYPROMELLOSE, MALTITOL, SAGE EXTRACT, XYLITOL, GREEN TEA EXTRACT, MENTHOL, MINT FLAVOR, PEACH FLAVOR, RED MINT FLAVOR, PEPPERMINT FLAVOR, ETC.

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73587-0020-12021-07-23C16284748780-1c7ccaba7-24b7-fd44-e053-dadaa90aa01b9e32f51e-8b9d-00bd-e053-2995a90abd79

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73587-0020-13SECONDS MAGIC GARGLE PEACH1 in 1 DOSE PACKTABLET11
73587-0020-13SECONDS MAGIC GARGLE PEACH18 in 1 BOXTABLET181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73587-00203SECONDS MAGIC GARGLE PEACH (SODIUM FLUORIDE) TABLET [SUNJINBIO CO.,LTD]1Legacy NDC, 2 package rows20200210_9e32f51e-8b9d-00bd-e053-2995a90abd79.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
73587-002073587-0020-1

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
XYLITOLVCQ006KQ1EIACT
MENTHOLL7T10EIP3AIACT
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
9e329c73-6fda-0f4d-e053-2995a90ab31c9e32f51e-8b9d-00bd-e053-2995a90abd792020-02-10WarningsExact identifier
spl id: 9e329c73-6fda-0f4d-e053-2995a90ab31c
spl set id: 9e32f51e-8b9d-00bd-e053-2995a90abd79

Reported adverse events (FAERS/openFDA)#

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