Label: FRESHMINT PREMIUM ANTICAVITY- sodium fluoride paste, dentifrice

  • NDC Code(s): 51824-029-01, 51824-029-02, 51824-029-03, 51824-029-04, view more
    51824-029-05, 51824-029-06, 51824-029-07
  • Packager: New World Imports, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 1, 2025

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  • OTC Active Ingredient

    Sodium Fluoride - 0.243% (0.15 w/v fluoride ion)

  • OTC Purpose

    Anticavity

  • Keep out of reach of Children under 6 years of age

    If you accidentally swallow more than used for brushing, seek professional help or contact a Poison Control Center immediately.

  • Uses

    Aids in the prevention of dental cavities

  • Warnings

    Keep out of reach of children under 6 years of age.if you accidentally swallow more than used for brushing, seek professional help or contact a Poison Control Center immediately.

  • Directions

    Adults and children 2 years & older:

    • Brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist.
    • Do not swallow.
    • Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing, use a pea-sized amount)
    • Supervise children's brushing until good habits are established.

    Children under 2 years:

    • Consult a dentist or doctor
  • Inactive Ingredients

    Sorbitol, Silica, Treated Water, Glycerin, PEG-32, Sodium Lauryl Sulfate, Flavor, Titanium Dioxide, Cellulose Gum, Carrageenan, Trisodium Phosphate, Sodium Saccharin, Sodium Benzoate, Tetrasodium Pyrophosphate, FD&C Blue #1

  • PRINCIPAL DISPLAY PANEL

    TPADA Tube

  • INGREDIENTS AND APPEARANCE
    FRESHMINT PREMIUM ANTICAVITY 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51824-029
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE2.43 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL 1600 (UNII: 1212Z7S33A)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    SODIUM PHOSPHATE, TRIBASIC, DODECAHYDRATE (UNII: B70850QPHR)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM SACCHARIN (UNII: SB8ZUX40TY)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    Colorblue (sky blue) Score    
    ShapeSize
    FlavorMINT (mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51824-029-02144 in 1 CARTON01/01/2013
    1NDC:51824-029-0124 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:51824-029-05144 in 1 CARTON01/01/2013
    2NDC:51824-029-0436 in 1 BOX
    2NDC:51824-029-0343 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:51824-029-0772 in 1 CARTON01/01/2013
    3NDC:51824-029-0685 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/01/2013
    Labeler - New World Imports, Inc (075372276)
    Registrant - New World Imports, Inc (075372276)
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