Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash

  • NDC Code(s): 59779-664-12, 59779-664-13, 59779-664-19, 59779-664-69, view more
    59779-664-77, 59779-664-86
  • Packager: CVS Pharmacy, Inc
  • 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 April 18, 2023

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  • Active ingredients

    Eucalyptol 0.092%

    Menthol 0.042%

    Methyl salicylate 0.060%

    Thymol 0.064%

  • Purpose

    Antigingivitis, antiplaque

  • Use

    help control plaque that leads to gingivitis

  • Warnings

    for this product

  • Do not use

    if you have painful or swollen gums, pus from the gum line, loose teeth or increased spacing between the teeth. See your dentist immediately. These may be signs of periodontitis, a serious form of gum disease.

  • Stop use and ask a dentist if

    gingivitis, bleeding, or redness persists for more than 2 weeks.

  • 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

    adults and children 12 years of age and older - vigorously swish 20 mL (2/3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds then spit out; do not swallow

    children unmder 12 years of age - consult a dentist or doctor

    • this rinse is not intended to replace brushing or flossing
  • Other information

    cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-77°F)

  • Inactive ingredients

    water, alcohol 21.6%, sorbitol solution, flavor, poloxamer 407, benzoic acid, sodium saccharin, sodium benzoate, green 3

  • Disclaimer

    This product is not manufactured or distributed by Johnson & Johnson Healthcare Products, distributor of Listerine Cool Mint Antiseptic

  • SPL UNCLASSIFIED SECTION

    Sealed with printed neckband for your protection. Do not use if broken or missing.

    This product is not manufactured or distributed by Johnson & Johnson Corporation, distributor of Cool Mint Listerine Antiseptic Mouthwash.

    Meets current TSA guidelines for carry-on luggage.

    Distributed by: CVS Pharmacy, Inc.

    One CVS Drive, Woonsacket, RI 02895

    (c) 2023 CVS Pharmacy, Inc.

    CVS.com  V-13687

    1-800-SHOP-CVS

    DSP-TN-21091

    DSP-MO-20087

  • principal display panel

    CVS

    Health

    Compare to the active ingredints in Listerine Cool Mint Antiseptic*

    Antiseptic

    Mouthwash

    ANTIGINGIVITIS/ANTIPLAQUE

    Kills gemrs that cause plaque, gingivitis & bad breath

    Blue Mint

    ADA

    Accepted

    American

    Dental

    Association

    • Helps prevent and reduce plaque
    • Helps prevent and reduce gingivitis

    3.2 FL OZ (94 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ANTISPETIC 
    eucalyptol, menthol, methyl salicylate, thymol mouthwash
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-664
    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 SALICYLATE0.60 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)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-664-69250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/1992
    2NDC:59779-664-1994 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/1992
    3NDC:59779-664-131250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/1992
    4NDC:59779-664-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/1992
    5NDC:59779-664-121500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/1992
    6NDC:59779-664-77500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/15/1992
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35609/15/1992
    Labeler - CVS Pharmacy, Inc (062312574)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(59779-664)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(59779-664)
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