Label: CREST PRO-HEALTH CLINICAL- cetylpyridinium chloride rinse

  • NDC Code(s): 37000-843-08, 37000-843-16, 37000-843-32
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 13, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Cetylpyridinium chloride 0.1%

  • Purpose

    Antigingivitis/Antiplaque

  • Uses

    • helps prevent and reduce plaque and gingivitis
    • helps control plaque bacteria that contribute to the development of gingivitis and bleeding gums
  • Warnings

    Ask a dentist if symptoms persist or condition worsens after regular use.

    Keep out of reach of children under 12 years of age. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • use after your normal brushing and flossing routine; rinse toothpaste from mouth prior to use
    • adults and children 12 yrs. & older: Rinse for 30 seconds with 20 mL (4 teaspoonfuls) twice a day
      • do not swallow
      • supervise use in children
    • children under 12 years of age: do not use
  • Inactive ingredients

    water, glycerin, hydrogen peroxide, flavor, sucralose, poloxamer 407

  • Questions?

    1–800–285–9139

  • SPL UNCLASSIFIED SECTION

    Dist. by Procter & Gamble,
    Cincinnati OH 45202

  • PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

    Crest®

    PRO-HEALTH™

    CPC ANTIGINGIVITIS/ANTIPLAQUE

    ORAL RINSE

    ALCOHOL FREE

    CLINICAL

    OUR MOST ADVANCED RINSE EVER

    • Reduces plaque & even helps prevent plaque regrowth
    • Helps prevent & even helps reverse gingivitis in 2 weeks
    • Kills 99% of germs to improve breath

    DEEP CLEAN MINT

    473mL

    (16 FL OZ)

    843

  • INGREDIENTS AND APPEARANCE
    CREST PRO-HEALTH  CLINICAL
    cetylpyridinium chloride rinse
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-843
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.02 g  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    Product Characteristics
    Colorwhite (Clear) Score    
    ShapeSize
    FlavorWINTERGREENImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-843-08237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/201102/10/2017
    2NDC:37000-843-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2011
    3NDC:37000-843-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/20/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02202/20/2011
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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