Label: LISTERINE CLINICAL SOLUTIONS GUM HEALTH ICY MINT- eucalyptol, menthol, methyl salicylate, thymol mouthwash

  • NDC Code(s): 69968-0818-1, 69968-0818-5, 69968-0818-9
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 4, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Eucalyptol (0.092%),

    Menthol (0.042%),

    Methyl Salicylate (0.060%),

    Thymol (0.064%)

  • Purposes

    Antiplaque/antigingivitis

  • Uses

    helps prevent and reduce:

    • plaque

    • gingivitis

  • Warnings

    Do not use in children under 12 years of age

    Ask a dentist if symptoms persist, new symptoms appear, or conditions worsen after regular use

    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

    • rinse full strength for 30 seconds with 20 mL (2/3 fluid ounce or 4 teaspoonfuls) morning and night

    • do not swallow

  • Other information

    • this rinse is not intended to replace brushing or flossing

    • store at room temperature

    • cold weather may cloud this product. Its antiseptic properties are not affected.

  • Inactive ingredients

    Water, Alcohol, Sorbitol, Poloxamer 407, Flavor, Zinc Chloride, Benzoic Acid, Sodium Benzoate, Sodium Saccharin, Sucralose, Red 40

  • Questions?

    call toll-free 888-222-0182 or 215-273-8755 (collect)

  • SPL UNCLASSIFIED SECTION

    Distributed by:

    JOHNSON & JOHNSON CONSUMER INC.

    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

    ANTIGINGIVITIS / ANTIPLAQUE MOUTHWASH

    LISTERINE ®

    CLINICAL

    SOLUTIONS

    ANTISEPTIC

    GUM HEALTH

    Immediately kills the germs that cause

    bleeding and inflammation for 3X healthier

    gums in one week* (*vs. brushing alone)

    ICY MINT

    1L (1 Qt 1.8 Fl Oz)

    Listerine_01

  • INGREDIENTS AND APPEARANCE
    LISTERINE CLINICAL SOLUTIONS GUM HEALTH ICY MINT 
    eucalyptol, menthol, methyl salicylate, thymol mouthwash
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0818
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL0.92 mg  in 1 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.42 mg  in 1 mL
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE0.6 mg  in 1 mL
    THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL0.64 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    SORBITOL (UNII: 506T60A25R)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    ZINC CHLORIDE (UNII: 86Q357L16B)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0818-995 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
    2NDC:69968-0818-5500 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
    3NDC:69968-0818-11000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/16/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02210/16/2023
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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