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

  • NDC Code(s): 11673-072-12, 11673-072-77
  • Packager: Target Corp
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 4, 2024

If you are a consumer or patient please visit this version.

  • Tamper Evident Statement 

    Sealed With Printed Neckband For Your Protection

  • Active ingredients

    Eucalyptol 0.092%

    Menthol 0.042%

    Methyl salicylate 0.060%

    Thymol 0.064%

  • Purpose

    Antigingivitis, Antiplaque

  • Use

    helps 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 under 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 (59⁰ - 77⁰F).

  • Inactive ingredients

    water, alcohol 21.6%, sorbitol, flavor, poloxamer 407, benzoic acid, sodium saccharin, sodium citrate, yellow 10, green 3

  • Questions or comments?

    Call 1-800-910-6874

  • Disclaimer

    *This product is not manufactured or distributed by Kenvue, Inc., distributor of FreshBurst ® Listerine  Antiseptic Mouthwash.

  • Adverse Reactions

    Distributed by Target Corporation

    Minneapolis, MN 55403

    Made in U.S. with U.S. and foreign components

    TM & ©2024 Target Brands, Inc.

    DSP-TN-21091

    DSP-MO-20087

  • Claims

    ADA Accepted

    American Dental Association

    • Helps prevent and reduce plaque
    • Helps prevent and reduce gingivitis
  • Principal display panel

    Compare to FreshBurst ® Listerine ®

    Antiseptic Mouthwash*

    Antiseptic Mouthwash

    Antigingivitis & Antiplaque

    Green Mint

    Twin Pack

    ADA Accepted

    American Dental Association

    Kills germs that cause bad breath, plaque and the gum disease gingivitis

    up & up

    1.5 L (1.58 QT) 50.7 FL OZ

    image description

  • INGREDIENTS AND APPEARANCE
    ANTISPETIC 
    eucalyptol, menthol, methyl salicylate, thymol mouthwash
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-072
    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 SOLUTION (UNII: 8KW3E207O2)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-072-121500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/08/1996
    2NDC:11673-072-77500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/08/1996
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/08/1996
    Labeler - Target Corp (006961700)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(11673-072)