Active ingredients

Potassium nitrate 5%
Sodium fluoride 0.25% (0.15% w/v fluoride ion)

Purposes

Antihypersensitivity
Anticavity

Uses

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

Warnings

Stop use and ask a dentist if

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

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 years of age and 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), 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.

Other information

do not store above 25°C (77°F)

Inactive ingredients

water, sorbitol, hydrated silica, glycerin, pentasodium triphosphate, PEG-8, sodium lauryl sulfate, flavor, alumina, titanium dioxide, xanthan gum, cocamidopropyl betaine, sodium hydroxide, carrageenan, sodium saccharin

Questions or comments?

1-866-844-2797

Additional Information (Enamel Strengthening)

ALWAYS FOLLOW THE LABEL

SENSODYNE CLINICAL WHITE

CLINICALLY PROVEN WHITENINGDESIGNED FOR SENSITIVE TEETH

WHITENING

Clinically proven whitening ingredients remove stains, polish teeth and help prevent future stains

SENSITIVITY PROTECTION

Clinically proven ingredients to protect against sensitivity and strengthen enamel.

Strengthens enamel

ENAMEL SAFE

* As shown in an 8 week study.
** With twice daily brushing.

Additional Information (Stain Protector)

ALWAYS FOLLOW THE LABEL

SENSODYNE

CLINICAL
WHITE

CLINICAL PROVEN
WHITENING
DESIGNED FOR
SENSITIVE TEETH

WHITENING
Clinically proven whitening ingredients remove stains, polish teeth and help prevent future stains

SENSITIVITY PROTECTION

Clinically proven ingredients to protect against sensitivity and strengthen enamel

Helps protect teeth from future stains

ENAMEL SAFE

* As shown in an 8 week study.
** With twice daily brushing.

Distributed by: Haleon, Warren, NJ 07059
Trademarks owned or licensed by Haleon.
© 2023 Haleon or licensor.

Principal Display Panel (Enamel Strengthening)

HALEON

TOOTHPASE FOR SENSITIVE TEETH AND CAVITY PREVENTION

SENSODYNE

2 SHADES WHITER TEETH*

+24/7 SENSITIVITY PROTECTION**

CLINICAL

WHITE

#1 DENTIST RECOMMENDED BRAND FOR SENSITIVE TEETH

ENAMEL STRENGTHENING

NET WT 5.5 OZ (156 g)

$Sensodyne Clinical White v3\Clin White Enam.jpg$

Principal Display Panel (Stain Protector)

NEW

#1 DENTIST RECOMMENDED BRAND FOR SENSITIVE TEETH

SENSODYNE

TOOTHPASTE FOR SENSITIVE TEETH AND CAVITY PREVENTION

2 SHADES WHITER TEETH*
+24/7 SENSITIVITY PROTECTION**

CLINICAL
WHITE

STAIN PROTECTOR

NET WT 3.4 OZ (96.4 g)

SENSODYNE CLINICAL WHITE STAIN PROTECTOR
potassium nitrate, sodium fluoride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0135-0702
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	50 mg in 1 g
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	2.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
SORBITOL (UNII: 506T60A25R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
ALUMINUM OXIDE (UNII: LMI26O6933)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
XANTHAN GUM (UNII: TTV12P4NEE)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODA LIME (UNII: 4RG4VJM6VG)
CARRAGEENAN (UNII: 5C69YCD2YJ)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0135-0702-01	1 in 1 CARTON	01/02/2024
1		96.4 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC:0135-0702-02	1 in 1 CARTON	01/02/2024
2		62.5 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC:0135-0702-03	1 in 1 CARTON	01/02/2024
3		23 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC:0135-0702-04	2 in 1 CARTON	01/02/2024
4		96.4 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M022	01/02/2024

SENSODYNE CLINICAL WHITE ENAMEL STRENGTHENING
potassium nitrate, sodium fluoride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0135-0703
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844)	POTASSIUM NITRATE	50 mg in 1 g
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	2.5 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
SORBITOL (UNII: 506T60A25R)
HYDRATED SILICA (UNII: Y6O7T4G8P9)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
ALUMINUM OXIDE (UNII: LMI26O6933)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
XANTHAN GUM (UNII: TTV12P4NEE)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODA LIME (UNII: 4RG4VJM6VG)
CARRAGEENAN (UNII: 5C69YCD2YJ)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)

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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0135-0703-01	1 in 1 CARTON	01/02/2024
1		96.4 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC:0135-0703-02	1 in 1 CARTON	01/02/2024
2		62.5 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC:0135-0703-05	1 in 1 CARTON	06/01/2025
3		156 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC:0135-0703-53	3 in 1 CARTON	06/01/2025
4		156 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M022	01/02/2024

Labeler - Haleon US Holdings LLC (079944263)

Name	Address	ID/FEI	Business Operations
Establishment
Haleon US Holdings LLC		046877908	analysis(0135-0703) , label(0135-0703) , manufacture(0135-0703)

Drug Facts

Active ingredients

Purposes

Uses

Warnings

Keep out of reach of children.

Directions

Other information

Inactive ingredients

Questions or comments?

Additional Information (Enamel Strengthening)

Additional Information (Stain Protector)

Principal Display Panel (Enamel Strengthening)

Principal Display Panel (Stain Protector)