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Dawnmist Fluoride (Dukal Corporation)

Available Formats

Dosage Form Package Information Links
PASTE 78 g in 1 TUBE (65517-1000-3) Label Information
PASTE 24 g in 1 TUBE (65517-1000-1) Label Information
PASTE 42 g in 1 TUBE (65517-1000-2) Label Information
PASTE 1 TUBE in 1 BOX (65517-1000-5) > 78 g in 1 TUBE Label Information
PASTE 1 TUBE in 1 BOX (65517-1000-7) > 181 g in 1 TUBE Label Information
PASTE 1 TUBE in 1 BOX (65517-1000-4) > 42 g in 1 TUBE Label Information
PASTE 17 g in 1 TUBE (65517-1000-0) Label Information
PASTE 1 TUBE in 1 BOX (65517-1000-6) > 135 g in 1 TUBE Label Information

Complete Dawnmist Fluoride Information

  • Active Ingredient

    Sodium Monofluorophosphate 0.76 percent


  • Purpose

    Anticavity


  • Use

    Aids in the prevention of dental cavities.


  • Keep out of reach of children

    under 6 years of age


  • Warning

    If you accidentally swallow more than used for brushing seek professional assistance or contact a Poison Control Center 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 sized amount and supervise brushing until good habits are established.

    Children under 2 years: Ask a dentist or physician.


  • Inactive Ingredients

    Calcium Carbonate, Water, Sorbitol, Hydrated Silica, Glycerin, Sodium Lauryl Sulfate, Flavor, Tetrasodium Pyrophosphate, Cellulose Gum, Sodium Benzoate, Sodium Saccharin


  • Package Label

    DawnMist (R)

    Anticavity Fluoride Toothpaste

    Cavity Fighting Formula

    Fresh Minty Taste

    Expiration Date: Expiration Date on Crimp of Tube.

    Manufactured for:

    DUKAL CORPORATION
    Ronkonkoma, NY 11779
    (631) 656-3800

    Made in Malaysia


    tube label

    box label


  • INGREDIENTS AND APPEARANCE
    DAWNMIST FLUORIDE  
    sodium monofluorophosphate paste
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:65517-1000
    Route of Administration DENTAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (MONOFLUOROPHOSPHATE ION - UNII:4964UZ79MI) SODIUM MONOFLUOROPHOSPHATE 0.76 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65517-1000-0 17 g in 1 TUBE
    2 NDC:65517-1000-1 24 g in 1 TUBE
    3 NDC:65517-1000-2 42 g in 1 TUBE
    4 NDC:65517-1000-3 78 g in 1 TUBE
    5 NDC:65517-1000-4 1 in 1 BOX
    5 42 g in 1 TUBE
    6 NDC:65517-1000-5 1 in 1 BOX
    6 78 g in 1 TUBE
    7 NDC:65517-1000-6 1 in 1 BOX
    7 135 g in 1 TUBE
    8 NDC:65517-1000-7 1 in 1 BOX
    8 181 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part355 09/24/2012
    Labeler - Dukal Corporation (791014871)