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

  • NDC Code(s): 0363-0318-69, 0363-0318-86, 0363-0318-88
  • Packager: Walgreen Co
  • 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 March 22, 2022

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

  • Safety Seal

    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 periodontist, a serious form of gum disease.

  • Stop use and ask a dentist

    gingivitis, bleeding, or redness persists for more thatn 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 teaspoonsfuls) 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 (59°-77°F).

  • Inactive ingredients

    water, alcohol 26.9%, benzoic acid, poloxamer 407, sodium benzoate, caramel

  • Questions or comments?

    1-800-925-4733

  • Adverse Reactions

    Our pharmacist recommend the Walgreens brand.  We invite you to compare to national brands.

    This product is not manufactured or distributed by Johnson & Johnson, owner of the registered trademark Listerine.

    DISTRIUBTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

    100% SATISFACTION GUARANTEED

    MADE IN U.S.A. WITH U.S. AD FOREIGN COMPONENTS

  • principal display panel

    Walgreens

    WALGREENS - PHARMACIST RECOMMENDED

    Compare to the active ingredients in Listerine Antiseptic

    Mouth Rinse

    ANTIGINGIVITIS/ANTIPLAQUE

    Antiseptic

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

    ADA

    Accepted

    American

    Dental

    Association

    • Helps reduce plaque
    • Helps reduce gingivitis

    33.8 FL OZ (1L)

    image description

  • INGREDIENTS AND APPEARANCE
    RINSE 
    eucalyptol, menthol, methyl salicylate, thymol mouthwash
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0318
    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)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CARAMEL (UNII: T9D99G2B1R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0318-69250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/1990
    2NDC:0363-0318-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/1990
    3NDC:0363-0318-882000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/15/1990
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35605/15/1990
    Labeler - Walgreen Co (008965063)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(0363-0318)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(0363-0318)