Label: CORINZ- cetylpyridinium chloride rinse

  • NDC Code(s): 53462-375-07, 53462-375-30, 53462-375-60
  • Packager: Sage Products, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2024

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  • Drug Facts

    Active ingredient: Purpose
    CORINZ ANTISEPTIC CLEANSING AND MOISTURIZING ORAL RINSE:
    Cetylpyridinium chloride 0.05%Antiseptic Rinse
  • Use

    Helps reduce chance of infection in minor oral irritation.

  • INDICATIONS & USAGE

  • Warnings

    Stop use and ask a doctor if:

    • Sore mouth symptoms do not improve in 7 days.
    • Swelling, rash or fever develops.
    • Irritation, pain or redness persists or worsens.
  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

  • Directions

    • Use up to 4 times daily or as directed by a dentist or doctor.
    • Adults and children 3 years and older: rinse mouth with 1/2 Tbsp. for approx. one minute. Instruct to expectorate.
    • Children under 3 years of age: consult a dentist or doctor.
  • Inactive ingredients

    Water, glycerin, xylitol, spearmint flavor, potassium sorbate, polysorbate 20, polysorbate 80, hydroethylcellulose, citric acid, sodium saccharin, menthol

  • Questions?

    800-323-2220.

  • SPL UNCLASSIFIED SECTION

    NOT MADE WITH NATURAL RUBBER LATEX • MADE IN U.S.A.

  • Corinz

    Corinz Bottle LabelCup LabelCorinz Packet (7 mL)

  • INGREDIENTS AND APPEARANCE
    CORINZ 
    cetylpyridinium chloride rinse
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53462-375
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3) CETYLPYRIDINIUM CHLORIDE0.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    XYLITOL (UNII: VCQ006KQ1E)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53462-375-607 mL in 1 PACKET; Type 0: Not a Combination Product01/20/2015
    2NDC:53462-375-077 mL in 1 CUP; Type 0: Not a Combination Product07/22/2019
    3NDC:53462-375-3044 mL in 1 BOTTLE; Type 0: Not a Combination Product04/07/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02201/20/2015
    Labeler - Sage Products, LLC (054326178)
    Registrant - Sage Products, LLC (054326178)
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