FDA.reportPublic FDA data

SEXYTEETHMINTTOOTHPASTE

Manufacturer
SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD
Effective date
2024-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:13:41

Label at a glance#

ProductSEXYTEETHMINTTOOTHPASTE
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

warningwarning

DOSAGE & ADMINISTRATION SECTION

dosagedosage

INACTIVE INGREDIENT SECTION

inactive ingredient sectioninactive ingredient section

INDICATIONS & USAGE SECTION

  • indications usage sectionindications usage section

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out reach of childrentkeep out reach of childrent

OTC - ACTIVE INGREDIENT SECTION

active ingdrentactive ingdrent

OTC - PURPOSE SECTION

purposepurpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416783sodium fluoride 0.24 % ToothpastePSN1
416783sodium fluoride 0.0024 MG/MG ToothpasteSCD1
416783sodium fluoride 0.24 % (fluoride ion 0.13 % ) ToothpasteSY1
416783sodium fluoride 0.24 % (fluoride ion 0.14 % ) ToothpasteSY1
416783sodium fluoride 0.24 % (fluoride ion 0.15 % ) ToothpasteSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74913-703-01SEXYTEETHMINTTOOTHPASTE113 g in 1 TUBEPASTE, DENTIFRICE1131

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74913-703SEXYTEETHMINTTOOTHPASTE (TOOTHPASTE) PASTE, DENTIFRICE [SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD]11 package rows20240616_1a30ed06-ec52-d94a-e063-6294a90ae8dc.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74913-70374913-703-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SORBITOL506T60A25RIACT
HYDRATED SILICAY6O7T4G8P9IACT
SPEARMINT OILC3M81465G5IACT
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM FLUORIDE8ZYQ1474W7ACTIB
GLYCERINPDC6A3C0OXIACT
XYLITOLVCQ006KQ1EIACT
STEVIA REBAUDIANA LEAF6TC6NN0876IACT
XANTHAN GUMTTV12P4NEEIACT

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
1a30ed06-ec53-d94a-e063-6294a90ae8dc1a30ed06-ec52-d94a-e063-6294a90ae8dc2024-06-05WarningsExact identifier
spl id: 1a30ed06-ec53-d94a-e063-6294a90ae8dc
spl set id: 1a30ed06-ec52-d94a-e063-6294a90ae8dc

Reported adverse events (FAERS/openFDA)#

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