FDA.reportPublic FDA data

Native

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2025-08-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 20:35:14

Label at a glance#

ProductNative Sensitivity
Active ingredientSODIUM FLUORIDE, POTASSIUM NITRATE
Label structure10 sections

Indications and uses

when used regularly, builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact aids in the prevention of cavities

Dosage and administration

adults and children 12 yrs. & older: apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth. do not swallow children under 12 yrs.: ask a dentist

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

5% potassium nitrate

0.243% sodium fluoride (0.14% w/v fluoride ion)

Purposes

OTC - PURPOSE SECTION

Toothpaste for sensitive teeth

Toothpaste for cavity prevention

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

OTC - WHEN USING SECTION

When using this product do not use for sensitivity longer than four weeks unless recommended by a dentist.

OTC - STOP USE SECTION

Stop use and ask a dentist if the sinsitivity problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 12 yrs. & older: apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth.
  • do not swallow
  • children under 12 yrs.: ask a dentist

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, water, hydrated silica, sodium cocoyl glutamate, flavor, mentha piperita (peppermint) oil, xanthan gum, carrageenan, stevia rebaudiana extract, titanium dioxide

Questions?

OTC - QUESTIONS SECTION

1-888-964-1211

SPL UNCLASSIFIED SECTION

Distr. by Native

San Francisco, CA 94111

PRINCIPAL DISPLAY PANEL - 116 g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WITH FLUORIDE

REDUCES SENSITIVITY

FRESHENS BREATH

FIGHTS CAVITIES

NATIVE

FLUORIDE TOOTHPASTE FOR SENSATIVE TEETH

NET WT 4.1 OZ (116g)

SENSITIVITY

SOOTHING MINT

69423-90369423-903

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
69423-90369423-903-41

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
STEVIA REBAUDIUNA LEAF6TC6NN0876IACT
GLYCERINPDC6A3C0OXIACT
HYDRATED SILICAY6O7T4G8P9IACT
SODIUM COCOYL GLUTAMATEBMT4RCZ3HGIACT
WATER059QF0KO0RIACT
XANTHAN GUMTTV12P4NEEIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
SODIUM FLUORIDE8ZYQ1474W7ACTIM
POTASSIUM NITRATERU45X2JN0ZACTIB
PEPPERMINT OILAV092KU4JHIACT

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
461369e0-d1d8-84e1-e063-6294a90a4972c1fb31f9-bbb1-71ee-e053-2a95a90abb2d2025-12-16WarningsExact identifier
spl set id: c1fb31f9-bbb1-71ee-e053-2a95a90abb2d

Reported adverse events (FAERS/openFDA)#

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