Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate and thymol mouthwash 

  • Label RSS
  • NDC Code(s): 0869-0664-12, 0869-0664-13, 0869-0664-19, 0869-0664-69, view more
    0869-0664-77, 0869-0664-86, 0869-0664-88
  • Packager: Vi-Jon
  • 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 02/13

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

  • Active ingredients

    Active ingredients

    Eucalyptol 0.0692%

    Menthol 0.042%

    Methyl salicylate 0.060%

    Thymol 0.064%

    Close
  • Purpose

    Purpose

    Antigingivitis, antiplaque

    Close
  • Use

    Use help control plaque that leads to gingivitis

    Close
  • Warnings

    Warnings

    Close
  • Do not use

    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

    Stop use and ask a dentist if gingivitis, bleeding, or redness persists for more than 2 weeks.

    Close
  • Keep out of reach of children.

    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.

    Close
  • Directions

    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 unmder 12 years of age - consult a dentist or doctor

    • this rinse is not intended to replace brushing or flossing
    Close
  • Inactive ingredients

    Inactive ingredients water, alcohol 21.6%, sorbitol solution, flavor, poloxamer 407, benzoic acid, sodium saccharin, sodium benzoate, FD+C green no.3

    Close
  • ADA Council Statement

    The ADA Council on scientific affairs Acceptanc of Safeway Blue Mint Antiseptic mouth rinse is based on its finding that the product is effective in helping to prevent and reduce gingivitis and plque above the gumline, when used as directed

    Close
  • Disclaimer

    This product is not manufactured or distribted by Johnson + Johnson Healthcare Products, distributor of Listerine

    Close
  • Adverse Reactions

    Distributed by: Vi-Jon

    One Swan Drive, Smyrna, TN 37167

    Close
  • Principal Display Panel

    Meets current TSA's guidelines for carry-on luggate

    Swan

    ANTISEPTIC

    MOUTH RINSE

    ice mint

    Kills Germs that

    Cause Bad Breath

    Plaque + the Gum

    Disease Gingivitis

    Compare to active ingredients

    of Listerine

    Sealed with printed neckband for your protection

    3.2 FL OZ (94 mL)

    image description

    Close
  • INGREDIENTS AND APPEARANCE
    ANTISPETIC 
    eucalyptol, menthol, methyl salicylate, thymol mouthwash
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:0869-0664
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    EUCALYPTOL (EUCALYPTOL) EUCALYPTOL 0.92 mg  in 1 mL
    MENTHOL (MENTHOL) MENTHOL 0.42 mg  in 1 mL
    METHYL SALICYLATE (SALICYLIC ACID) METHYL SALICYLATE 0.60 mg  in 1 mL
    THYMOL (THYMOL) THYMOL 0.64 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    SORBITOL  
    POLOXAMER 407  
    BENZOIC ACID  
    SACCHARIN SODIUM  
    SODIUM BENZOATE  
    FD&C GREEN NO. 3  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0869-0664-86 1000 mL in 1 BOTTLE, PLASTIC
    2 NDC:0869-0664-77 500 mL in 1 BOTTLE, PLASTIC
    3 NDC:0869-0664-69 250 mL in 1 BOTTLE, PLASTIC
    4 NDC:0869-0664-88 2000 mL in 1 BOTTLE, PLASTIC
    5 NDC:0869-0664-13 1250 mL in 1 BOTTLE, PLASTIC
    6 NDC:0869-0664-12 1250 mL in 1 BOTTLE, PLASTIC
    7 NDC:0869-0664-19 94 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part356 07/15/1992
    Labeler - Vi-Jon (790752542)
    Registrant - Vi-Jon (790752542)
    Establishment
    Name Address ID/FEI Business Operations
    Vi-Jon 790752542 manufacture(0869-0664)
    Close