Label: ANTISEPTIC MOUTH RINSE- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 71141-157-12, 71141-157-32
- Packager: Lidl US, LLC
- 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 6, 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 if
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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SPL UNCLASSIFIED SECTION
*This product is not manufactued or distributed by Johnson & Johnson Corporation., owner of the registered trademark Listerine.
DISTRIBUTED BY
Lidl US, LLC
Arlington, VA 22202
QUESTIONS?
1-844-5071
www.Lidl.com
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item replaced
DSP-TN-21091 DSP-MO-20087
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Discard seal, empty & Replace Cap
Plastic bottle
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Principal Panel Display
SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION
Kills Germs That Cause Bad Breath, Plaque, & Gingivitis Gum Disease
ANTISEPTIC
MOUTHWASH
ORIGINAL AMBER
ADA
ACCEPTED
American
Dental
Association
- Helps reduce plaque
- Helps reduce gingivitis
Compare to Original Listerine Antiseptic Mouthwash
ANTI-GINGIVITIS/ANTI-PLAQUE
MOUTHWASH
1.0 L (1 QT 1.8 FL OZ)
-
Principal Panel Display
dentaux
by LIDL
ORIGINAL
ANTI-GINGIVITIS/ANTI-PLAQUE
MOUTHWASH
ANTISEPTIC
MOUTHWASH
ADA
ACCEPTED
American
Dental Association
- Helps prevent and redice plaque
- Helps prevent and redice gingivitis
SEALED WITH PRINTED NECKBAND
FOR YOUR PROTECTION
Kills Germs that Cause Plaque, Gingivitis, Bad Breath
NDC-71141-157-12
50.7 FL OZ (1.58 QT) 1.5L
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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:71141-157 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:71141-157-32 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/09/2017 2 NDC:71141-157-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/09/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 02/09/2017 Labeler - Lidl US, LLC (079389709) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(71141-157) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(71141-157)