FDA.reportPublic FDA data

Superba

Manufacturer
Dollar Shave Club, Inc.
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:45:01

Label at a glance#

ProductSuperba
Active ingredientSODIUM FLUORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Sodium fluoride 0.234%

OTC - PURPOSE SECTION

Purpose Anticavity

INDICATIONS & USAGE SECTION

Use Aids in the prevention of dental cavities

WARNINGS SECTION

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Twist off cap to remove foil seal. Do not use if safety seal is missing or boken.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Do not swallow.
  • Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise chldren as necessary until capable of using without supervision.
  • Children under 2 years of age: Consult a dentist or a doctor.

INACTIVE INGREDIENT SECTION

Inactive Ingredients Sorbitol, Water/Aqua/Eau, Hydrated Silica, Glycerin, Xylitol, Cocamidopropyl Betain, Flavor (Aroma), Xanthan Gum, Titanium Dioxide (CI 77891), Stevia Rebaudiana Extract, Limonene, Linalool.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SUPERBA

PEPPERMINT KICK

FLUORIDE TOOTHPASTE

SULFATE-FREE

NET WT 5.0 OZ (142g)

MANUFACTURED FOR

DOLLAR SHAVE CLUB, INC.

LOS ANGELES, CA 90292

MADE IN SPAIN

LABELLABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2585483sodium fluoride 0.234 % ToothpastePSN1
2585483sodium fluoride 0.00234 MG/MG ToothpasteSCD1
2585483sodium fluoride 0.234 % ToothpasteSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69522-1113-12023-01-30C16284748780-1f386c649-c94e-0266-e053-dadaa90a7c1aDollar Shave Club Superba toothpaste

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69522-1113-1Superba142 g in 1 TUBEPASTE1421

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69522-1113SUPERBA (SODIUM FLUORIDE) PASTE [DOLLAR SHAVE CLUB, INC.]1Legacy NDC, 1 package rows20211121_cfd30151-44a8-97b9-e053-2995a90a4b0f.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69522-111369522-1113-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
SORBITOL506T60A25RIACT
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
XYLITOLVCQ006KQ1EIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LINALOOL, (+)-F4VNO44C09IACT
SODIUM FLUORIDE8ZYQ1474W7ACTIM
WATER059QF0KO0RIACT
HYDRATED SILICAY6O7T4G8P9IACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
LIMONENE, (+)-GFD7C86Q1WIACT

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
cfd30151-44a9-97b9-e053-2995a90a4b0fcfd30151-44a8-97b9-e053-2995a90a4b0f2021-11-02WarningsExact identifier
spl id: cfd30151-44a9-97b9-e053-2995a90a4b0f
spl set id: cfd30151-44a8-97b9-e053-2995a90a4b0f

Reported adverse events (FAERS/openFDA)#

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