Label: MORNING FRESH MINT TOOTHPASTE, WITH FLUORIDE paste

  • NDC Code(s): 67777-190-01, 67777-190-02, 67777-190-03, 67777-190-04, view more
    67777-190-05, 67777-190-06, 67777-190-07, 67777-190-08, 67777-190-09
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 7, 2026

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  • Active Ingredient

    Sodium Monofluorophosphate 0.76% (0.13% w/v fluoride ion)

  • Purpose

    Anticavity

  • Use(s)

    Helps protect against cavities

  • Warning

    Do Not Swallow

    Keep out of reach of children under 6 years of age

    If you accidentally swallow more than used for brushing, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

  • Directions

    • Adults 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: to minimize swallowing, use a pea size amount and supervise brushing and rinsing until good habits are established.

    • Children under 2 years: Use as directed by a dentist or physician.

  • Inactive Ingredients

    Calcium Carbonate, Carboxymethylcellulose Sodium, Methylparaben, Peppermint Oil, Polyethylene Glycol 400, Propylparaben, Purified Water, Saccharin Sodium, Silicon Dioxide, Sodium Benzoate, Sodium Lauryl Sulfate, Sodium Pyrophosphate, Sodium Silicate, Sorbitol, Titanium Dioxide

  • Other Information

    Store between 15º - 35ºC (59º - 95ºF)

  • Questions?

    1-888-396-2739 Monday - Friday 9AM - 5PM EST

  • Label

    4871 BX MASTER4871 Label

  • Label

    4872 BX MASTER4872 Label

  • Label

    4873 BX MASTER4873 Label

  • INGREDIENTS AND APPEARANCE
    MORNING FRESH MINT TOOTHPASTE, WITH FLUORIDE 
    morning fresh mint toothpaste, with fluoride paste
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-190
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM SILICATE (UNII: IJF18F77L3)  
    WATER (UNII: 059QF0KO0R)  
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-190-035 in 1 CASE01/15/2025
    1NDC:67777-190-02144 in 1 BOX
    1NDC:67777-190-0125.14 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:67777-190-06144 in 1 CASE01/15/2025
    2NDC:67777-190-051 in 1 BOX
    2NDC:67777-190-0444.36 mL in 1 TUBE; Type 0: Not a Combination Product
    3NDC:67777-190-09144 in 1 CASE01/15/2025
    3NDC:67777-190-081 in 1 BOX
    3NDC:67777-190-0781.33 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/15/2025
    Labeler - Dynarex Corporation (008124539)
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