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

  • NDC Code(s): 69423-767-27, 69423-767-28, 69423-767-29, 69423-767-38, view more
    69423-767-39, 69423-767-76
  • 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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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Sodium fluoride 0.243% (0.15% w/v fluoride ion)

  • Purpose

    Anticavity toothpaste

  • Use

    helps protect against cavities

  • Warning

    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

    water, sorbitol, hydrated silica, disodium
    pyrophosphate, sodium lauryl sulfate, sodium hydroxide, flavor, cellulose gum,
    sodium saccharin, carbomer, charcoal powder, polysorbate 80, mica, titanium
    dioxide

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 76 g Tube Carton

    Crest

    3D White

    Advanced

    Charcoal

    NET WT 2.7 OZ (76 g)

    Fluoride Anticavity Toothpaste

    Enamel Safe Whitening

    Removes 90% more

    Surface Stains*

    Starts Whitening After 1 Brush

    artwork

  • INGREDIENTS AND APPEARANCE
    CREST 3D WHITE  ADVANCED CHARCOAL
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-767
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    SORBITOL (UNII: 506T60A25R)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    MICA (UNII: V8A1AW0880)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    Product Characteristics
    ColorblackScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-767-282 in 1 CELLO PACK02/17/2023
    11 in 1 CARTON
    176 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:69423-767-381 in 1 CARTON02/17/2023
    2107 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:69423-767-762 in 1 CARTON02/17/2023
    3107 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:69423-767-271 in 1 CARTON02/17/2023
    476 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:69423-767-293 in 1 CELLO PACK02/17/202307/19/2023
    51 in 1 CARTON
    576 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:69423-767-393 in 1 CELLO PACK02/17/2023
    61 in 1 CARTON
    6107 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02102/17/2023
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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