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 July 15, 2024
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- Official Label (Printer Friendly)
- TEP
- 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 (c) 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.
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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 (1L)
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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 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 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)