Label: CREST COMPLETE MULTI-BENEFIT WHITENING PLUS CINNAMON EXPRESSIONS- sodium fluoride gel, dentifrice

  • NDC Code(s): 37000-826-04
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 13, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Sodium fluoride 0.243%

  • Purpose

    Anticavity toothpaste

  • Use

    helps protect against cavities

  • Warnings

    Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
      • do not swallow
      • to minimize swallowing use a pea-sized amount in children under 6
      • supervise children's brushing until good habits are established
    • children under 2 yrs.: ask a dentist
  • Inactive ingredients

    sorbitol, water, hydrated silica, tetrasodium pyrophosphate, PEG-6, glycerin, sodium lauryl sulfate, disodium pyrophosphate, flavor, sodium saccharin, cellulose gum, carnauba wax, carbomer, titanium dioxide, red 40

  • Questions?

    1-800-285-3213

  • SPL UNCLASSIFIED SECTION

    Dist. by Procter & Gamble,
    Cincinnati, OH 45202

  • PRINCIPAL DISPLAY PANEL - 130 g Bottle Label

    WHITENING+

    CINNAMON
    EXPRESSIONS

    cinnamon
    rush™
    liquid gel

    Fights Cavities,
    Whitens + Bold
    Cinnamon Flavor

    Crest®
    complete
    MULTI-BENEFIT™

    FLUORIDE TOOTHPASTE

    NET WT
    4.6 OZ (130 g)

    99606202

    Principal Display Panel - 130 g Bottle Label
  • INGREDIENTS AND APPEARANCE
    CREST COMPLETE MULTI-BENEFIT  WHITENING PLUS CINNAMON EXPRESSIONS
    sodium fluoride gel, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-826
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorCINNAMONImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-826-04130 g in 1 BOTTLE; Type 0: Not a Combination Product07/01/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02107/01/2011
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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