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

  • NDC Code(s): 69423-770-22, 69423-770-27, 69423-770-33, 69423-770-38, view more
    69423-770-40, 69423-770-56, 69423-770-85, 69423-770-92
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 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

  • 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, flavor, sodium hydroxide, cellulose gum,
    sodium saccharin, carbomer, polysorbate 80, mica, titanium dioxide, blue 1

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 24 g Tube Carton

    CREST

    3D WHITE

    ADVANCED

    RADIANT MINT

    net wt 0.85 oz (24 g)

    fluoride anticavity toothpaste

    ENAMEL SAFE WHITENING

    REMOVES 90% MORE SURFACE STAINS*

    artwork

  • INGREDIENTS AND APPEARANCE
    CREST 3D WHITE  ADVANCED RADIANT MINT
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-770
    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
    MICA (UNII: V8A1AW0880)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-770-851 in 1 CARTON08/01/2021
    124 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:69423-770-271 in 1 CARTON08/01/2021
    276 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:69423-770-403 in 1 CELLO PACK10/11/2020
    31 in 1 CARTON
    3107 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:69423-770-561 in 1 CARTON08/01/2021
    4158 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:69423-770-222 in 1 CARTON08/01/2021
    576 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:69423-770-922 in 1 CELLO PACK10/11/2020
    61 in 1 CARTON
    6107 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:69423-770-381 in 1 CARTON08/01/2021
    7107 g in 1 TUBE; Type 0: Not a Combination Product
    8NDC:69423-770-331 in 1 CARTON10/11/2020
    899 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02110/11/2020
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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