Label: QUALITY CHOICE MINT- cetylpryidinium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 14, 2015

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  • Active ingredients

    Cetylpyridinium Chloride 0.07%

    Purpose

    Antiplaque/Antigingivitis

  • Uses

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

    Ask 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 immediately (1-800-222-1222)

  • Directions

    • Use after your normal brushing and flossing routine; rinse toothpaste from mouth prior to use
    • Adults and children 6 years and 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.
  • Other information

    Store at room temperature

  • Inactive ingredients

    Water (Aqua), Glycerin, Poloxamer 407, Flavor, Sodium Saccharin, Methylparaben, Sucralose, Propylparaben, Blue 1 (CI 42090)

  • Questions or comments?

    1-248-449-9300

  • Label Copy

    Image of the label

  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE MINT 
    cetylpryidinium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-553
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.7 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-553-331000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35609/13/2015
    Labeler - CHAIN DRUG MARKETING ASSOCIATION INC (011920774)
    Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    APOLLO HEALTH AND BEAUTY CARE201901209manufacture(63868-553)
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