Native by The Procter & Gamble Manufacturing Company Native Sensitivity

Native by

Drug Labeling and Warnings

Native by is a Otc medication manufactured, distributed, or labeled by The Procter & Gamble Manufacturing Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NATIVE SENSITIVITY- potassium nitrate, sodium fluoride paste, dentifrice 
The Procter & Gamble Manufacturing Company

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Native Sensitivity

Drug Facts

Active ingredient

5% potassium nitrate

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

Purposes

Toothpaste for sensitive teeth

Toothpaste for cavity prevention

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

Warnings

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

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.

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

• 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

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

Questions?

1-888-964-1211

Distr. by Native

San Francisco, CA 94111

PRINCIPAL DISPLAY PANEL - 116 g Tube Carton

WITH FLUORIDE

REDUCES SENSITIVITY

FRESHENS BREATH

FIGHTS CAVITIES

NATIVE

FLUORIDE TOOTHPASTE FOR SENSATIVE TEETH

NET WT 4.1 OZ (116g)

SENSITIVITY

SOOTHING MINT

NATIVE  SENSITIVITY
potassium nitrate, sodium fluoride paste, dentifrice

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69423-903
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	1.4 mg  in 1 g
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
GLYCERIN (UNII: PDC6A3C0OX)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
WATER (UNII: 059QF0KO0R)
XANTHAN GUM (UNII: TTV12P4NEE)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
PEPPERMINT OIL (UNII: AV092KU4JH)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	MINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69423-903-41	1 in 1 CARTON	05/10/2021
1		116 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M021	05/10/2021	12/31/2024

Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 12/2025

Document Id: 461369e0-d1d8-84e1-e063-6294a90a4972

34390-5

Set id: c1fb31f9-bbb1-71ee-e053-2a95a90abb2d

Version: 6

Effective Time: 20251216

 

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