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

  • NDC Code(s): 37808-664-12, 37808-664-69, 37808-664-77, 37808-664-86
  • Packager: H-E-B
  • 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 June 28, 2022

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%

  • Purpose

    Antigingivitis, antiplaque

  • Use

    help control plaque that leads to gingivitis

  • Warnings

    ​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

     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.  Its antiseptic properties are not affected.  Store at (59° - 77°F).

  • Inactive ingredients

    water, alcohol (21.6%), sorbitol solution, flavor, poloxamer 407, benzoic acid, sodium saccharin, sodium benzoate, FD&C green no. 3

  • Questions?

    Call 1-888-593-0593

  • SPL UNCLASSIFIED SECTION

    SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION.

    The ADA Council on Scientific Affairs Acceptance of HEB Cool Blue Mint Antiseptic Mouthwash 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.

    *This product is not manufactured or distributed by Johnson & Johnson Healthcare Products, distributor of Listerine Mouthwash.

    MADE WITH PRIDE AND CARE FOR H-E-B

    San Antonio, TX 78204

  • Principal Display Panel

    Compare to Listerine*

    H-E-B COOL BLUE MINT ANTISEPTIC

    ANTIGINGIVITIS/ANTIPLAQUE

    MOUTHWASH

    ADA Accepted American Dental Association

    • Helps Fight Germs That Causes Bad Breath
    • Fights Plaque & Gingivitis

    50.7 FL OZ (1.58 QT) 1.5 L

    image description

  • INGREDIENTS AND APPEARANCE
    ANTISPETIC 
    eucalyptol, menthol, methyl salicylate, thymol mouthwash
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37808-664
    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)  
    SORBITOL (UNII: 506T60A25R)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37808-664-121500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/19/2009
    2NDC:37808-664-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/19/2009
    3NDC:37808-664-77500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/19/2009
    4NDC:37808-664-69250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/19/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35605/19/2009
    Labeler - H-E-B (007924756)
    Registrant - Vi-Jon (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon790752542manufacture(37808-664)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon088520668manufacture(37808-664)