Label: CREST PRO HEALTH WHITENING GEL- stannous fluoride paste, dentifrice

  • NDC Code(s): 69423-786-03, 69423-786-43, 69423-786-44, 69423-786-45, view more
    69423-786-46, 69423-786-59
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 6, 2024

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  • Drug Facts

    Active ingredient

    Stannous fluoride 0.454%

    (0.15% w/v fluoride ion)

  • Purposes

    Anticavity, antigingivitis, antisensitivity toothpaste

  • Uses

    • aids in the prevention of cavities
    • helps prevent gingivitis
    • helps interfere with the harmful effects of plaque associated with gingivitis
    • helps control plaque bacteria that contribute to the development of gingivitis
    • builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact
  • WARNINGS

    Warnings

    When using this product do not use for sensitivity longer than four weeks unless recommended by a dentist.

    Stop use and ask a dentist if the sensitivity problem persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care.

    Keep out of reach of children. 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: apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth.
    • do not swallow
    • children under 12 yrs. of age: ask a dentist
  • Other information

    • products containing stannous fluoride may produce surface staining of the teeth
    • adequate toothbrushing may prevent these stains which are not harmful or permanent and may be removed by your dentist
    • this Crest is specially formulated to help prevent staining
    • see your dentist regularly
  • Inactive ingredients

    water, sorbitol, hydrated silica, sodium lauryl sulfate, sodium gluconate, carrageenan, flavor, sodium citrate, xanthan gum, zinc citrate, glycine, sodium hydroxide, stannous chloride, sodium saccharin, sucralose, mica, titanium dioxide, blue 1

  • Questions?

    1-800-594-4158

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE,

    CINCINNATI, OH 45202

  • Principal Display Panel - 167 g tube in carton

    69423-786Crest

    PRO-HEALTH

    FLUORIDE TOOTHPASTE FOR ANTICAVITY, ANTIGINGIVITIS AND SENSITIVE TEETH

    CAVITIES GUM ENAMEL SENSITIVITY PLAQUE TARTAR WHITENS FRESHENS BREATH

    NET WT 5.9 OZ (167 g)

    FORMULATED WITH AMINO ACID GLYCINE

    WHITENING

    PROTECTS 100%

    OF THE WHOLE MOUTH

  • INGREDIENTS AND APPEARANCE
    CREST  PRO HEALTH WHITENING GEL
    stannous fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-786
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    STANNOUS CHLORIDE (UNII: 1BQV3749L5)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    SORBITOL (UNII: 506T60A25R)  
    GLYCINE (UNII: TE7660XO1C)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    ZINC CITRATE (UNII: K72I3DEX9B)  
    MICA (UNII: V8A1AW0880)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-786-431 in 1 CARTON12/30/2022
    1121 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:69423-786-442 in 1 CARTON12/30/2022
    2121 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:69423-786-453 in 1 CARTON12/30/2022
    3121 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:69423-786-591 in 1 CARTON12/30/2022
    4167 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:69423-786-031 in 1 CARTON12/30/2022
    585 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:69423-786-461 in 1 CARTON12/30/2022
    6130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02112/30/2022
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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