Label: ANTISEPTIC- eucalyptol, menthol, methyl salicylate, thymol liquid

  • NDC Code(s): 79903-152-75, 79903-152-99
  • Packager: WALMART INC. (see also Equate)
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 22, 2024

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  • Active ingredient

    Eucalyptol (0.092%)

    Menthol (0.042%)

    Methyl Salicylate (0.060%)

    Thymol (0.064%)

  • Purposes

    Antiplaque/antigingivitis

  • Uses

    helps prevent and reduce

    • plaque
    • gingivitis
  • Warning

    Do not use

    in children under 12 years of age.

    Stop use and ask a dentist

    • gingivitis, bleeding, or redness persists for more than 2 weeks
    • you have painful or swollen gums, pus from the gum line, loose teeth, or increasing spacing between the teeth. These may be signs or symptoms of periodontitis, a serious form of gum disease.

    Keep out of reach of children under 6 years of age

    If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away

  • Directions

    • adults and children 12 years of age and older: vigorously swish 20 milliliters of rinse between your teeth twice a day for 30 seconds and then spit out. Do not swallow the rinse.
    • children 6 years to under 12 years of age: supervise use
    • children under 6 years of age: do not use
  • Other information

    • store at room temperature
    • cold weather may cloud this product. Its antiseptic properties are not affected.
    • this rinse is not intended to replace brushing or flossing
  • Inactive ingredients

    water, alcohol (21.6% v/v), sorbitol, poloxamer 407, sodium benzoate, benzoic acid, sodium saccharin, flavor, D&C yellow #10, FD&C green #3

  • Questions or comments

    1-888-287-1915

  • Principal display panel

    Compare to Listerine® Freshburst® active ingredients*

    Antiseptic Mouthwash

    Green Mint

    Kills germs that cause plaque, gingivitis bad breath

    Help to control and prevent plaque that leads to gingivitis

    Eucalyptol (0.092%)

    Menthol (0.042%)

    Methyl salicylate (0.060%)

    Thymol (0.064%)

    Antiplaque/antigingivitis

    L (QT PT FL OZ)

    *This product is not manufactured or distributed by Johnson & Johnson Consumer Inc., distributor of Listerine® Freshburst®.

    TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE OR UNDER CAP IS BROKEN OR MISSING.

    DISTRIBUTED BY: Walmart Inc.,

    Bentonville, AR 72716

  • Package label

    Eucalyptol (0.092%) Menthol (0.042%) Methyl Salicylate (0.060%) Thymol (0.064%)

    EQUATE Antiseptic Mouthwash Green Mint

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC 
    eucalyptol, menthol, methyl salicylate, thymol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-152
    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)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-152-751500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/30/2022
    2NDC:79903-152-992 in 1 PACKAGE12/30/2022
    21500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02212/30/2022
    Labeler - WALMART INC. (see also Equate) (051957769)
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