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
- 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 9, 2023
If you are a consumer or patient please visit this version.
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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 0.60 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 not final part356 05/15/1990 Labeler - Walgreen Co (008965063) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0363-0318) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(0363-0318)