Label: ANTISEPTIC MOUTH RINSE- eucalyptol mouthwash

  • NDC Code(s): 0363-0072-12, 0363-0072-13, 0363-0072-69, 0363-0072-77, view more
    0363-0072-86, 0363-0072-88
  • Packager: Walgreens Co.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 17, 2024

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  • 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

    • do not swallow
    • not intended to replace brushing or flossing

    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

    Children under 12 years of age - Consult a dentist or doctor

  • Other information

    Store at room temperature (59⁰ - 77⁰F)

  • Inactive ingredients

    water, alcohol 21.6%, sorbitol solution, flavor, poloxamer 407, benzoic acid, sodium saccharin, flavor, sodium citrate, yellow 10,  green3

  • Disclaimer

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

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

    walgreens.com 1-800-925-4733

    W3ORG0924-F

    DSP-TN-21081 DSP-MO-80087

    ITEM 771870 W10100-1024-F

  • principal display panel

    SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION

    Walgreens

    NEW

    Compare to the active ingredients in Freshburst® Listerine® Antiseptic Mouthwash‡

    Mouth Rinse

    ANTIGINGIVITIS/ANTIPLAQUE

    Antiseptic

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

    ADA Accepted

    American Dental Association

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

    8.5 FL OZ (250 mL)

    Mint flavor

    image description

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC MOUTH RINSE 
    eucalyptol mouthwash
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0072
    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)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINT (Spring Mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0072-77500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    2NDC:0363-0072-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    3NDC:0363-0072-121500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    4NDC:0363-0072-131250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    5NDC:0363-0072-882000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    6NDC:0363-0072-69250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/30/2007
    Labeler - Walgreens Co. (008965063)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(0363-0072)
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