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
  • 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 February 4, 2022

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

  • TEP

    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 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

    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
  • Other information

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

  • Inactive ingredients

    water, alcohol 21.6%, sorbitol, flavor, poloxamer 407, benzoic acid, sodium saccharin, sodium citrate, yellow 10,  green 3

  • Disclaimer

    Our pharmacists recommend the Walgreens brand.  We invite you to compare to nation brands.

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

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

    100% SATISFACTION GUARANTEED  

    walgreens.com 

    2021 Walgreen Co.

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

  • principal display panel

    WALGREENS - PHARMACIST RECOMMENDED

    Walgreens

    Compare to the active ingredients in Listine Freshburts

    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 (1 L)

    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) EUCALYPTOL0.092 kg  in 100 L
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.042 kg  in 100 L
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE0.060 kg  in 100 L
    THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL0.064 kg  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINT (Spring Mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-0072-770.5 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    2NDC:0363-0072-861 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    3NDC:0363-0072-121.5 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    4NDC:0363-0072-131.25 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    5NDC:0363-0072-882 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2007
    6NDC:0363-0072-69.25 L 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 not finalpart34803/30/2007
    Labeler - Walgreens Co. (008965063)
    Registrant - Vi Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC790752542manufacture(0363-0072)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC088520668manufacture(0363-0072)