Label: ANTISEPTIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 11673-318-12
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
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 March 21, 2022
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- 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
- Adverse reaction section
- Disclaimer
- ADA Council Statement
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principal display panel
SAFETY SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION
ADA
Accepted
American
Dental Association
antiseptic mouthwash
Antigingivitis/Antiplaque
Compare to Listerine Antiseptic Original
Kills germs that cause bad breath, plaque and the gum disease gingivitis
ORIGINAL
FLAVOR
up & up
50.7 FL OZ (1.5 L)
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INGREDIENTS AND APPEARANCE
ANTISEPTIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-318 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:11673-318-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/1996 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 07/15/1996 Labeler - Target Corporation (006961700) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(11673-318) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(11673-318)