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
Drug Label Information
Updated April 23, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Tamper Evident Statement
- Active ingredients
- Purpose
- Use
- Warnings
- Do not use
- Stop use and ask a dentist if
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Adverse Reactions
DISTRIUBTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com ©2021 Walgreen Co.
MADE IN U.S.A. WITH U.S. AD FOREIGN COMPONENTS
†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 ®.
Empty & Replace Cap
PLASTIC BOTTLE
how2recycle.info
DSP-TN-21091
DSP-MO-20087
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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 (1 L)


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INGREDIENTS AND APPEARANCE
RINSE
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0318 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength EUCALYPTOL (UNII: RV6J6604TK) (EUCALYPTOL - UNII:RV6J6604TK) EUCALYPTOL 0.92 mg in 1 mL MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.42 mg in 1 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 0.6 mg in 1 mL THYMOL (UNII: 3J50XA376E) (THYMOL - UNII:3J50XA376E) THYMOL 0.64 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) BENZOIC ACID (UNII: 8SKN0B0MIM) POLOXAMER 407 (UNII: TUF2IVW3M2) SODIUM BENZOATE (UNII: OJ245FE5EU) CARAMEL (UNII: T9D99G2B1R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0318-69 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/15/1990 05/25/2017 2 NDC:0363-0318-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/15/1990 3 NDC:0363-0318-88 2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/15/1990 08/13/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 05/15/1990 Labeler - Walgreen Co (008965063) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(0363-0318)
