Label: CREST SCOPE ADVANCED- sodium fluoride rinse

  • NDC Code(s): 37000-208-05, 37000-208-10
  • 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 0.02% (0.01% w/v fluoride ion)

  • Purpose

    Anticavity

  • Use

    Aids in the prevention of dental cavities

  • Warnings

    Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Adults and children 6 years & older: Use twice a day after brushing your teeth with a toothpaste.
    • Vigorously swish 10 mL (2teaspoonfuls) of rinse between your teeth for 1 minute and then spit out.
    • Do not swallow the rinse.
    • Do not eat or drink for 30 minutes after rinsing.
    • Instruct children under 12 years of age in good rinsing habits (to minimize swallowing).
    • Supervise children as necessary until capable of using without supervision.
    • Children under 6 years of age: Consult a dentist or doctor.
  • Inactive ingredients

    water, alcohol (15 wt%), propylene glycol, flavor, benzoic acid, poloxamer 407, cetylpyridinium chloride, sucralose, phosphoric acid, disodium phosphate, yellow 5, blue 1

  • Questions?

    1-800-862-7442

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE,
    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 1000mL Bottle Label

    Crest®
    ANTICAVITY FLUORIDE MOUTHWASH
    scope®

    ADVANCED™

    MULTI-ACTION FORMULA

    +FLOURIDE

    • HELPS PREVENT CAVITIES
    • FORTIFIES ENAMEL
    • FRESHENS BREATH
    • CLEANS WHOLE MOUTH

    IMPORTANT: Read directions for proper use.
    SEE BACK FOR IMPORTANT INGREDIENT INFORMATION.

    1L (33.8 FL OZ)

    LABELS

  • INGREDIENTS AND APPEARANCE
    CREST SCOPE  ADVANCED
    sodium fluoride rinse
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-208
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    PHOSPHORIC ACID (UNII: E4GA8884NN)  
    ALCOHOL (UNII: 3K9958V90M)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-208-05500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2019
    2NDC:37000-208-101000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/01/2019
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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