Label: EVO SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT- potassium nitrate, sodium fluoride paste, dentifrice

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 13, 2025

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  • Drug Facts

  • Active ingredients

    Potassium Nitrate 5%
    Sodium Fluoride 0.24%
    (0.14% w/v fluoride ion)

  • Purpose

    Antihypersensitivity
    Anticavity

  • Uses

    helps in the prevention of dental decay

  • Warnings

    Do not use if you are allergic to any of the ingredients.

    Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, call Poison Help at 1-800-222-1222 or go to PoisonHelp.org.

  • Directions

    • Do not swallow

    • Supervise children as necessary until capable of using without supervision

    • Adult and children 2 years and older
      brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician

    • Children under 6 years
      instruct in good brushing and rinsing habits (to minimize swallowing)

    • Children under 2 years
      ask a dentist or physician

  • Inactive ingredients

    Calcium Carbonate, Aqua (Water), Sorbitol, Silica, Sodium Lauryl Sulfate, Flavor, PEG-8, Benzyl Alcohol, Cellulose Gum, Xanthan Gum, Sodium Saccharin, Sodium Benzoate, Titanium Dioxide, Sodium Silicate

  • Questions or comments?

    Call toll free 1-877-274-8358

  • SPL UNCLASSIFIED SECTION

    FRESHENS BREATH

    HELPS PREVENT CAVITIES

    STRENGTHENS TEETH WITH ACTIVE FLUORIDE

    DESIGNED IN U.S.A.
    MADE IN INDIA

    GETEVO.NET

    1-909-434-0911 INTERNATIONAL

    PATENTS, COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE
    DISTRIBUTED BY ASHTEL STUDIOS INC.
    ONTARIO, CALIFORNIA 91761

  • Packaging

    evo ANTI-CAVITY FLUORIDE SWEET MINT

  • INGREDIENTS AND APPEARANCE
    EVO SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT 
    potassium nitrate, sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70108-254
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE5 g  in 100 g
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.24 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SODIUM SILICATE (UNII: IJF18F77L3)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINT (Sweet Mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70108-254-011 in 1 BOX10/01/2025
    199 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02210/01/2025
    Labeler - Ashtel Studios, Inc. (148689180)
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