Label: FRESHEN UP- sodium fluoride, potassium nitrate gel, dentifrice

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

Drug Label Information

Updated July 14, 2026

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Sodium Monofluorophosphate (0.76%)........Anticavity

    Total Fluoride content- 1000 ppm appx.

  • Purpose

    Anticavity

  • Use

    helps protect against cavities

  • Warnings

    Stop use and ask a dentist if the problem persists or worsens, snesitive teeth may indicate a serious problem that may need prompt care by dentist. Pain senstivity still persists after 4 weeks of use

    Keep out of reach of children under 6 years of age.If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    adults and children 2 years of age and olderbrush teeth thoroughly, preferably after each meal or at least twice a day or as directed by physician or dentist
    children 2 to 6 yearsuse only a pea siz amount and supervise child's brushing and rinsing (to minimize swallowing)
    children under 2 yearsask a dentist or physician
  • Inactive ingredients

    calcium carbonate, water, sorbitol, silica, SLS, flavor, sodium silicate, tetrasodium pyrophosphate, xanthum gum, sodium carboxymethylcellulose, benzyl alcohol, sodium benzoate, sodium bicarbonate, sodium saccharin, titanium dioxide, peg-400, blue 1

  • Questions?

    1-888-880-1504

  • SPL UNCLASSIFIED SECTION

    Dist. by:
    MKJ Brands

  • PRINCIPAL DISPLAY PANEL

    col (1)

  • INGREDIENTS AND APPEARANCE
    FRESHEN UP 
    sodium fluoride, potassium nitrate gel, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77782-005
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.76 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM SACCHARIN (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    PEG-400 (UNII: 2AS3MDK9CB)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    TETRASODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SODIUM SILICATE (UNII: IJF18F77L3)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CI 42090 (UNII: H3R47K3TBD)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77782-005-202 in 1 BOX01/02/2026
    199 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/02/2026
    Labeler - MKJ BRANDS LLC (827648101)
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