Label: ANTISEPTIC MOUTH RINSE- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 30142-318-12, 30142-318-77, 30142-318-86
- Packager: Kroger 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 7, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Use
- Warnings
- Do not use
- Stop use and ask a dentist
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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SPL UNCLASSIFIED SECTION
*Listerine is a registered trademark of Johnson & Johnson Healthcare Products,
Skillman, NJ 08558. Johnson & Johnson Healthcare Products is not
affiliated wth The Kroger Co. or this product.
DISTRIBUTED BY THE KROGER CO.
CINCINNATI, OHIO 45202
QUALITY GUARANTEE
800-632-6900 www.kroger.com
DSP-TN-21091
DSP-MO-20087
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Principal display panel
COMPARE to the active ingredients of ORIGINAL LISTERINE
*See Back Label
KROGER
Original
ANTISEPTIC
MOUTH RINSE
ANTIGINGIVITIS/ANTIPLAQUE
- Kills Germs That Cause Bad Breath, Plaque & the Gum Disease Gingivitis
- For Fresher Breath
SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION
ADA Accepted
American Dental Association
- Helps prevent and reduce plaque
- Helps prevent and reduce gingivitis
16.9 FL OZ (500 mL)
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INGREDIENTS AND APPEARANCE
ANTISEPTIC MOUTH RINSE
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-318 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:30142-318-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/15/1991 2 NDC:30142-318-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/15/1991 3 NDC:30142-318-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/15/1991 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 06/15/1991 Labeler - Kroger Co (006999528) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(30142-318) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(30142-318)