Label: GELATO NEUTRAL PH- sodium fluoride gel 

  • Label RSS
  • NDC Code(s): 68400-136-15
  • Packager: Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 11/13

If you are a consumer or patient please visit this version.

  • Active Ingredient: 

    Sodium Fluoride 2%

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  • Purpose:

    Fluoride treatment gel.

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  • Indications and Usage:

    • A stable thixotropic fluoride treatment gel used to help prevent dental decay.
    • For Professional Use Only. This product is not intended for home or unsupervised consumer use.
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  • Warnings:

    • Keep out of reach of children.
    • Do not swallow. If product is accidentally swallowed in quantities greater than would normally occur with a treatment gel, seek medical help or contact a poison control center right away.
    • Read directions carefully before using.
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  • Dosage and Administration:

    Shake well before use. This is a four minute fluoride gel for in-office patient use. It is normally used as a preventative caries treatment two times a year.

    1. After thorough prophylaxis, fill two single or one dual tray, one third full with gel. Air dry teeth and insert trays into the mouth.

    2. Instruct patient to bite down lightly but firmly for four minutes.

    3. Remove trays. Instruct patient to expectorate any excess gel and not to eat or drink for at least 30 minutes.

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  • Other Infomation:

    Store at controlled room temperature 59° to 86°F (15°-30°C).

    Protect from freezing.

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  • Inactive Ingredients:

    Citric Acid, Flavor, Magnesium Aluminum Silicate, Phosphoric Acid, Polysorbate 20, Potassium Hydroxide, Sodium Benzoate, Sodium Saccharin, Titanium Dioxide, Water, Xanthan Gum, Xylitol.

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  • INGREDIENTS AND APPEARANCE
    GELATO NEUTRAL PH 
    sodium fluoride gel
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:68400-136
    Route of Administration DENTAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION 4.086 g  in 454 g
    Inactive Ingredients
    Ingredient Name Strength
    CITRIC ACID MONOHYDRATE  
    MAGNESIUM ALUMINUM SILICATE  
    PHOSPHORIC ACID  
    POLYSORBATE 20  
    POTASSIUM HYDROXIDE  
    SODIUM BENZOATE  
    SACCHARIN SODIUM  
    TITANIUM DIOXIDE  
    WATER  
    XANTHAN GUM  
    XYLITOL  
    Product Characteristics
    Color white (Dye Free) Score     
    Shape Size
    Flavor MINT Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68400-136-15 454 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 03/01/2013
    Labeler - Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc (078654194)
    Establishment
    Name Address ID/FEI Business Operations
    Mycone Dental Supply Co., Inc DBA Keystone Industries and Deepak Products Inc 078654194 manufacture(68400-136), label(68400-136)
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