Label: CREST COMPLETE MULTI BENEFIT WHITENING PLUS SCOPE OUTLAST- sodium fluoride paste, dentifrice

  • NDC Code(s): 37000-504-05, 37000-504-12, 37000-504-40, 37000-504-48, view more
    37000-504-54, 37000-504-58, 37000-504-73, 37000-504-76, 37000-504-80, 37000-504-98, 37000-504-99
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 18, 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

  • 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

    sorbitol, water, hydrated silica, disodium pyrophosphate, flavor, sodium lauryl sulfate, sodium hydroxide, alcohol (0.7%), xanthan gum, sodium saccharin, glycerin, carbomer, poloxamer 407, polysorbate 80, sodium benzoate, cetylpyridinium chloride, benzoic acid, mica, titanium dioxide, blue 1, yellow 5

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE,
    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 164 g Carton

    SUGAR SHIELD | STRENGTHENS AREAS WEAKENED BY SUGAR

    Crest ®

    complete

    MULTI-BENEFIT™

    NET WT 5.8 OZ (164 g)

    FLUORIDE TOOTHPASTE

    WHITENING +
    scope
    OUTLAST     ®

    FEEL FRESH UP TO 7X LONGER

    504

  • INGREDIENTS AND APPEARANCE
    CREST COMPLETE MULTI BENEFIT  WHITENING PLUS SCOPE OUTLAST
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-504
    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 BENZOATE (UNII: OJ245FE5EU)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    SORBITOL (UNII: 506T60A25R)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    MICA (UNII: V8A1AW0880)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    ALCOHOL (UNII: 3K9958V90M)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    Product Characteristics
    Colorwhite (with green stripe) Score    
    ShapeSize
    FlavorPEPPERMINT, WINTERGREENImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-504-401 in 1 CARTON09/08/2009
    1113 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:37000-504-581 in 1 CARTON09/08/2009
    2164 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:37000-504-761 in 1 CARTON09/08/200906/14/2019
    3215 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:37000-504-122 in 1 CARTON09/08/200906/14/2019
    4164 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:37000-504-055 in 1 CELLO PACK09/08/2009
    51 in 1 CARTON
    5206 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:37000-504-982 in 1 CARTON01/01/2019
    6153 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:37000-504-993 in 1 CELLO PACK01/01/2019
    71 in 1 CARTON
    7153 g in 1 TUBE; Type 0: Not a Combination Product
    8NDC:37000-504-541 in 1 CARTON01/01/2019
    8153 g in 1 TUBE; Type 0: Not a Combination Product
    9NDC:37000-504-801 in 1 CARTON01/01/2019
    9226 g in 1 TUBE; Type 0: Not a Combination Product
    10NDC:37000-504-731 in 1 CARTON09/08/2009
    10206 g in 1 TUBE; Type 0: Not a Combination Product
    11NDC:37000-504-481 in 1 CARTON09/08/2009
    11136 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02109/08/2009
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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