Label: FLUORIDE - sodium fluoride tablet, chewable 

  • Label RSS
  • NDC Code(s): 51862-171-10, 51862-171-12
  • Packager: Libertas Pharma, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 08/12

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  • DESCRIPTION

    Active Ingredient: 0.5 mg of fluoride ion from 1.1 mg of sodium fluoride (NaF).

    Inactive Ingredients: Lactose, Saccharine, Grape Flavor and Magnesium Stearate.

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  • DOSAGE AND ADMINISTRATION:

    Dissolve in the mouth or chew before swallowing, preferably at bedtime after brushing teeth.

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  • STORAGE:

    Store at a Controlled Room Temperature 20º-25ºC (68º-77ºF)

    743633

    Manufactured for:
    Libertas Pharma, Inc.
    Lawrenceville, GA 30043
    Iss. 03/11   171-10

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  • Container Label

    NDC 51862-171-10

    Fluoride Chewable Tablets

    0.5 mg

    (From 1.1 mg of Sodium Fluoride)

    Grape Flavor       1000 Tablets       Rx Only

    Libertas
    Pharma Inc.

    Container Label

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  • INGREDIENTS AND APPEARANCE
    FLUORIDE 
    fluoride tablet, chewable
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:51862-171
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION 0.5 mg
    Inactive Ingredients
    Ingredient Name Strength
    GRAPE  
    LACTOSE  
    SACCHARIN  
    MAGNESIUM STEARATE  
    Product Characteristics
    Color PURPLE Score no score
    Shape ROUND Size 6mm
    Flavor GRAPE Imprint Code 171
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51862-171-10 1000 in 1 BOTTLE
    2 NDC:51862-171-12 120 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved drug other 05/21/2011
    Labeler - Libertas Pharma, Inc. (962128943)
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