Label: CREST 3D WHITE WHITENING THERAPY DEEP CLEAN CHARCOAL- sodium fluoride paste, dentifrice

  • NDC Code(s): 37000-215-03, 37000-215-04, 37000-215-24, 37000-215-28, view more
    37000-215-35, 37000-215-41, 37000-215-52, 37000-215-60, 37000-215-82, 37000-215-85
  • Packager: Procter & Gamble Manfuacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 13, 2024

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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

  • 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

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

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE,

    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 116 g Carton

    Crest®

    3D WHITE™

    FLUORIDE ANTICAVITY TOOTHPASTE

    WHITENING

    THERAPY™

    charcoal

    DEEP CLEAN

    INVIGORATING MINT

    NET WT 4.1 OZ (116 g)

    215

  • INGREDIENTS AND APPEARANCE
    CREST 3D WHITE WHITENING THERAPY  DEEP CLEAN CHARCOAL
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-215
    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
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    MICA (UNII: V8A1AW0880)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorPEPPERMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-215-411 in 1 CARTON01/01/2019
    1116 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:37000-215-822 in 1 CELLO PACK01/01/2019
    21 in 1 CARTON
    2116 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:37000-215-281 in 1 CARTON01/01/202007/20/2023
    379 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:37000-215-851 in 1 CARTON01/01/2020
    424 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:37000-215-521 in 1 CARTON01/01/2020
    5147 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:37000-215-033 in 1 CELLO PACK01/01/201907/20/2023
    61 in 1 CARTON
    6147 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:37000-215-044 in 1 CELLO PACK01/01/201907/20/2023
    71 in 1 CARTON
    7147 g in 1 TUBE; Type 0: Not a Combination Product
    8NDC:37000-215-241 in 1 CARTON01/01/2020
    868 g in 1 TUBE; Type 0: Not a Combination Product
    9NDC:37000-215-351 in 1 CARTON01/01/2019
    999 g in 1 TUBE; Type 0: Not a Combination Product
    10NDC:37000-215-602 in 1 CELLO PACK01/01/2019
    101 in 1 CARTON
    1099 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/01/2019
    Labeler - Procter & Gamble Manfuacturing Company (004238200)
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