Label: CREST PRO-HEALTH INTENSE CLEAN MINT- cetylpyridinium chloride rinse

  • NDC Code(s): 37000-479-05, 37000-479-10, 37000-479-36
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 8, 2025

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Cetylpyridinium chloride 0.05%

  • 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 6 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 6 yrs. & older: Rinse for 30 seconds with 20 mL (4 teaspoonfuls) twice a day
      • do not swallow
      • children 6 years to under 12 years of age: supervise use
    • children under 6 years of age: do not use
  • Inactive ingredients

    water, alcohol (15 wt%), propylene glycol, flavor, poloxamer 407, sucralose, benzoic acid, sodium benzoate, blue 1, yellow 6

  • Questions?

    1–800–285–9139

  • PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label

    COOLING

    SENSATION

    Crest®
    PRO-HEALTH™
    CPC ANTIGINGIVITIS/ANTIPLAQUE ORAL MOUTHWASH

    INTENSE

    99% GERM KILL

    CLEAN MINT

    • KEEPS TEETH CLEANER LONGER*
    • FRESHENS BREATH
    • FIGHTS PLAQUE & GINGIVITIS

    See back for important

    ingredient information.

    500 mL

    (16.9 FL OZ)

    479

  • INGREDIENTS AND APPEARANCE
    CREST PRO-HEALTH  INTENSE CLEAN MINT
    cetylpyridinium chloride rinse
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-479
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.05 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    ALCOHOL (UNII: 3K9958V90M)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37000-479-05500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2018
    2NDC:37000-479-101000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2018
    3NDC:37000-479-3636 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02201/01/2018
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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