Label: CREST PRO-HEALTH SENSITIVITY RELIEF- sodium fluoride and potassium nitrate paste, dentifrice

  • NDC Code(s): 84126-639-05, 84126-639-51
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 10, 2026

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Potassium nitrate 5%Toothpaste for sensitive teeth
    Sodium fluoride 0.243% (0.14% w/v fluoride ion)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 productdo not use longer than four weeks unless recommended by a dentist.

    Stop use and ask a dentist ifproblem lasts or gets worse. 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

    • 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
    • do not use in children under 12 yrs.
  • Inactive ingredients

    water, hydrated silica, glycerin, sorbitol, sodium lauryl sulfate,
    trisodium phosphate, flavor, cellulose gum, alcohol (0.7%), sodium saccharin, xanthan
    gum, polysorbate 80, cetylpyridinium chloride, titanium dioxide, blue 1

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    Dist. by Procter & Gamble, Cincinnati, OH 45202

  • PRINCIPAL DISPLAY PANEL - 170 g Tube Carton

    Crest

    PRO-HEALTH

    NET WT

    5.1 0Z (144 g)

    TOOTHPASTE FOR SENSITIVE TEETH AND CAVITY PROTECTION

    DENTIST DESIGNED

    CLINICALLY PROVEN

    + WHITENING

    SENSITIVITY RELIEF

    Maximum strength** sensitivity relief

    MINTY FRESH SCOPE

    label

  • INGREDIENTS AND APPEARANCE
    CREST PRO-HEALTH  SENSITIVITY RELIEF
    sodium fluoride and potassium nitrate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-639
    Route of AdministrationDENTAL
    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 ION1.4 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CELLULOSE GUM (UNII: K679OBS311)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    ALCOHOL (UNII: 3K9958V90M)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84126-639-511 in 1 CARTON01/06/2026
    1144 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:84126-639-052 in 1 CARTON01/06/2026
    2144 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/06/2026
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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