Label: COLGATE MAXFRESH FRESH MINT- sodium fluoride gel, dentifrice 

  • Label RSS
  • NDC Code(s): 65954-010-81
  • Packager: Mission Hills S.A de C.V
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 02/14

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

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  • Active Ingredient

    Sodium fluoride 0.24% (0.14% w/v fluoride ion)

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  • Purpose

    Anticavity

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  • Use

    helps protect against cavities

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  • Warnings

    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.

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  • Directions

    adults and children 2 years of age and older brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician
    children 2 to 6 years use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing)
    children under 2 years ask a dentist or physician
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  • Inactive Ingredients

    sorbitol, water, hydrated silica, PEG-12, sodium lauryl sulfate, tetrasodium pyrophosphate, flavor, cocamidopropyl betaine, sodium saccharin, cellulose gum, xanthan gum, mica, titanium dioxide, FD&C blue no. 1

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  • Questions?

    1-800-468-6502

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  • SPL UNCLASSIFIED SECTION

    Dist. by:
    COLGATE-PALMOLIVE COMPANY
    New York, NY 10022

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  • PRINCIPAL DISPLAY PANEL - 130 g Bottle Label

    1D

    Colgate®

    Fluoride Toothpaste

    1D

    Fresh Mint

    NET WT 4.6 OZ (130g) LIQUID GEL

    Principal Display Panel - 130 g Bottle Label
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  • INGREDIENTS AND APPEARANCE
    COLGATE MAXFRESH FRESH MINT 
    sodium fluoride gel, dentifrice
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:65954-010
    Route of Administration DENTAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION 1.1 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    SORBITOL 670 mg  in 1 g
    WATER  
    HYDRATED SILICA  
    POLYETHYLENE GLYCOL 600  
    SODIUM LAURYL SULFATE  
    SODIUM PYROPHOSPHATE  
    COCAMIDOPROPYL BETAINE  
    SACCHARIN SODIUM  
    CARBOXYMETHYLCELLULOSE SODIUM  
    XANTHAN GUM  
    MICA  
    TITANIUM DIOXIDE  
    FD&C BLUE NO. 1  
    Product Characteristics
    Color BLUE Score     
    Shape Size
    Flavor MINT Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65954-010-81 130 g in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part355 01/08/2013
    Labeler - Mission Hills S.A de C.V (812312122)
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