Label: CREST 3D WHITE ADVANCED- sodium monofluorophosphate paste, dentifrice

  • NDC Code(s): 69423-752-30
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 12, 2023

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  • Drug Facts

    Sodium monofluorophosphate 1.14%

    (0.17% w/v fluoride ion)

  • Purpose

    Anticavity toothpaste

  • Use

    helps protect against cavities

  • WARNINGS

  • Warning

    Keep out of reach of children under 12 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 12 yrs. & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.
    • do not swallow
    • children under 12 yrs.: ask a dentist
  • Inactive ingredients

    water, glycerin, calcium pyrophosphate, hydrogen peroxide (2.5% w/v), sodium lauryl sulfate, flavor, polyacrylate crosspolymer-6, cetearyl alcohol, disodium pyrophosphate, tetrasodium pyrophosphate, sucralose

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

  • Crest 3D White Ultra White 85g tube in carton

    Crest

    3D WHITE

    FLUORIDE ANTICAVITY TOOTHPASTE

    ADVANCED HYDROGEN PEROXIDE

    2.5%

    WHITENS* AND DEEPLY CLEANS

    *BY REMOVING SURFACE STAINS

    FRESH MINT

    ENAMEL SAFE WHITENING

    NET WT 3.0 OZ (85 g)

    artwork

  • INGREDIENTS AND APPEARANCE
    CREST 3D WHITE ADVANCED 
    sodium monofluorophosphate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-752
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.7 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    CALCIUM PYROPHOSPHATE (UNII: X69NU20D19)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    WATER (UNII: 059QF0KO0R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-752-301 in 1 CARTON01/10/2023
    185 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02201/10/2023
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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