Goodsense Sensitive Extra Whitening

Manufacturer
Geiss, Destin & Dunn, Inc.
Effective date
2017-12-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:53:25

Label at a glance#

ProductGoodsense Sensitive Extra Whitening
Active ingredientPOTASSIUM NITRATE, SODIUM FLUORIDE
Label structure9 sections

Storage and handling

Other information store below 30°C (86°F) Lot No. & Exp. Date: see box or see crimp of tube

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients                                                               Purpose

Potassium nitrate 5%........................................ Antihypersensitivity

Sodium fluoride 0.15% w/v fluoride ion..............................Anticavity

OTC - PURPOSE SECTION

Uses

  • builds increasing protection against painful sensitivity of the teeth due to cold, heat, acids, sweets or contact
  • aids in the prevention of dental cavities

WARNINGS SECTION

Warnings

Stop use and ask a dentist if

  • the problem persists or worsens. Sensitive teeth may indicate a serious problem that may prompt care by a dentist
  • pain/sensitivty still persists after 4 weeks of use

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 accidently swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

Directions

  • adults and children 12 years of age and older
  • appy at least 1-inch strip of product onto a soft bristle toothbrush
  • brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Minimize swallowing. Spit out after brushing.
  • children under 12 years of age: consult a dentist or doctor

STORAGE AND HANDLING SECTION

Other information

  • store below 30°C (86°F)
  • Lot No. & Exp. Date: see box or see crimp of tube

INACTIVE INGREDIENT SECTION

Inactive ingredients sorbitol, water, hydrated silica, cocamidopropyl betaine, PEG 1500, flavor, cellulose gum, titanium dioxide, sodium saccharin, menthol, tetrasodium pyrophosphate

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Geiss, Destin & Dunn, Inc.

Peachtree City, GA 30269

Made in Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038800potassium nitrate 5 % / sodium fluoride 0.243 % (fluoride ion 0.14 % - 0.15 % ) ToothpastePSN2
1038800potassium nitrate 0.05 MG/MG / sodium fluoride 0.00243 MG/MG ToothpasteSCD2
1038800K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.00243 MG/MG ToothpasteSY2
1038800Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.00243 MG/MG ToothpasteSY2
1038800potassium nitrate 5 % / sodium fluoride 0.243 % (fluoride ion 0.15 % ) ToothpasteSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50804-780-042020-01-31C16284748780-19d75b9d0-6e5f-f424-e053-dadaa90a57ceGoodsense Sensitive Toothpaste Extra Whitening 4 oz NBE Sensodyne

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-780-04Goodsense Sensitive Extra Whitening1 in 1 BOXPASTE12
50804-780-04Goodsense Sensitive Extra Whitening113 g in 1 TUBEPASTE1132

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50804-780GOODSENSE SENSITIVE EXTRA WHITENING (POTASSIUM NITRATE, AND SODIUM FLUROIDE) PASTE [GEISS, DESTIN & DUNN, INC.]2Legacy NDC, 2 package rows20171213_a5634768-18f3-433b-9480-420ccc97d80f.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
50804-78050804-780-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML · Source PDF

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
602d5713-f692-17cc-e053-2a91aa0a2d77a5634768-18f3-433b-9480-420ccc97d80f2017-12-12WarningsExact identifier
spl id: 602d5713-f692-17cc-e053-2a91aa0a2d77
spl set id: a5634768-18f3-433b-9480-420ccc97d80f

Reported adverse events (FAERS/openFDA)#

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