Label: ANTISEPTIC MOUTH RINSE- eucalyptol, menthol, methyl salicylate and thymol mouthwash 

  • Label RSS
  • 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
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 04/13

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

  • Active ingredients


    Eucalyptol 0.092%  Menthol 0.042%   Methyl salicylate 0.060%  Thymol  0.064%

    Close
  • Purpose

    Antigingivitis, Antiplaque

    Close
  • Use

     helps control plaque that leads to gingivitis

    Close
  • WARNINGS

    Warnings

    Close
  • 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.

    Close
  • Stop use and ask a dentist if 

    Gingivitis, bleeding or redness persists for more than 2 weeks

    Close
  • Keep out of reach of children

    Of more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

    Close
  • 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
    Close
  • Other information

    cold weather may cloud this product.  It antiseptic properties are not affected.  Store at room temperature (59⁰ - 77⁰ F)

    Close
  • Inactive ingredients

    water, alcohol 21.6%, sorbitol, flavor, poloxamer 407, benzoic acid, sodium saccharin, sodium citrate, D+C yellow no. 10, FD+C green no.3

    Close
  • ADA Council Statement

    The ADA Council on Scientific  Affairs Acceptance of  Wallgreens Spring Mint Antiseptic Mouth Rinse is based on its finding that the product is effective in helping to prevent and reduce gingivitis and plaque above the gumline, when used as directed.

    Close
  • Disclaimer and other information

    This proeuct is not manufactured or distributed by Johnson + Johnson Healthcare products, distributor of Listerine Fresh Burst

    DSP-TN-1500  DSP-MO-34  SDS-TN-15012

    Close
  • Adverse Reactions Section

    QUESTION OR COMMENTS? 1-888-593-0593

    DISTRIBUTED BY: WALGREEN CO

    200 WILMOT RD, DEERFIELD, IL 60015

    1005 SATISFACTION GUARANTEED

    walgreens.com

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

    Close
  • Principal Display Panel

    WELL at 

    Walgreens

    ANTISEPTIC

    Mouth Rinse

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

    ADA

    Accepted

    American

    Dental

    Association

    Spring Mint

    Compare to Listerine Fresh Burst Active ingredients

    33.8 FL OZ (1L)

    image description

    Close
  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC MOUTH RINSE 
    eucalyptol mouthwash
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:0363-0072
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EUCALYPTOL (EUCALYPTOL) EUCALYPTOL 0.092 kg  in 100 L
    MENTHOL (MENTHOL) MENTHOL 0.042 kg  in 100 L
    METHYL SALICYLATE (SALICYLIC ACID) METHYL SALICYLATE 0.060 kg  in 100 L
    THYMOL (THYMOL) THYMOL 0.064 kg  in 100 L
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL  
    POLOXAMER 407  
    BENZOIC ACID  
    SODIUM CITRATE  
    Product Characteristics
    Color      Score     
    Shape Size
    Flavor MINT (Spring Mint) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0363-0072-77 0.5 L in 1 BOTTLE, PLASTIC
    2 NDC:0363-0072-86 1 L in 1 BOTTLE, PLASTIC
    3 NDC:0363-0072-12 1.5 L in 1 BOTTLE, PLASTIC
    4 NDC:0363-0072-13 1.25 L in 1 BOTTLE, PLASTIC
    5 NDC:0363-0072-88 2 L in 1 BOTTLE, PLASTIC
    6 NDC:0363-0072-69 .25 L in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part348 03/30/2007
    Labeler - Walgreens Co. (008965063)
    Registrant - Vi Jon (790752542)
    Establishment
    Name Address ID/FEI Business Operations
    Vi Jon 790752542 manufacture(0363-0072)
    Close