Label: SENSODYNE CLINICAL WHITE STAIN PROTECTOR- potassium nitrate, sodium fluoride paste
SENSODYNE CLINICAL WHITE ENAMEL STRENGTHENING- potassium nitrate, sodium fluoride paste

  • NDC Code(s): 0135-0702-01, 0135-0702-02, 0135-0702-03, 0135-0702-04, view more
    0135-0703-01, 0135-0703-02
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 4, 2024

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  • 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 thorough 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

  • Other (Enamel Strengthening)

    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

    Strengthens enamel

    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.

  • Other (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)

    NEW

    #1 DENTIST RECOMMENDED BRAND FOR SENSITIVE TEETH

    SENSODYNE

    TOOTHPASE FOR SENSITIVE TEETH AND CAVITY PREVENTION

    2 SHADES WHITER TEETH*

    +24/7 SENSITIVITY PROTECTION**

    CLINICAL

    WHITE

    ENAMEL STRENGTHENING

    NET WT 2.3 OZ (65.2 g)

    Clinical White Enamel Strengthening 65.2 g
  • 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)

    Clinical White Stain Protector 96.4g
  • INGREDIENTS AND APPEARANCE
    SENSODYNE  CLINICAL WHITE STAIN PROTECTOR
    potassium nitrate, sodium fluoride paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0702
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE50 mg  in 1 g
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION2.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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
    ColorwhiteScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-0702-011 in 1 CARTON01/02/2024
    196.4 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:0135-0702-021 in 1 CARTON01/02/2024
    262.5 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:0135-0702-031 in 1 CARTON01/02/2024
    323 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:0135-0702-042 in 1 CARTON01/02/2024
    496.4 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02201/02/2024
    SENSODYNE  CLINICAL WHITE ENAMEL STRENGTHENING
    potassium nitrate, sodium fluoride paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0703
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE50 mg  in 1 g
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION2.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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
    ColorwhiteScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-0703-011 in 1 CARTON01/02/2024
    196.4 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:0135-0703-021 in 1 CARTON01/02/2024
    262.5 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02201/02/2024
    Labeler - Haleon US Holdings LLC (079944263)
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