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
  • 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 January 26, 2023

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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 citrate, flavor, benzoic acid, sodium saccharin, yellow #10, green #3

  • Questions or comments

    1-888-287-1915

  • Principal display panel

    Compare to Listerine® Freshburst® active ingredients*

    Antiseptic Mouthwash

    Eucalyptol (0.092%)

    Menthol (0.042%)

    Methyl salicylate (0.060%)

    Thymol (0.064%)

    Antiplaque/antigingivitis

    • Kills germs that cause plaque, gingivitis, bad breath
    • Help to control and prevent plaque that leads to gingivitis

    Mint Blast

    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 Mint Blast

  • 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)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    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 not finalpart35612/30/2022
    Labeler - WALMART INC. (see also Equate) (051957769)
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