Label: ANTISEPTIC MOUTHRINSE- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 49035-072-12, 49035-072-69, 49035-072-77, 49035-072-86
- Packager: Wal-Mart Stores, Inc.
- 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 February 2, 2023
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- Official Label (Printer Friendly)
- TEP
- Active ingredients
- Purpose
- Use
- Warnings
- Do not use if
- Stop use and ask a dentist if
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Satisfaction guaranteed
- Adverse Reactions Section
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Principal Display Panel
NDC: 49035-072-12
equate
Compare to FreshBurst Listerine Active Ingredients*
Antiseptic Mouthrinse
Kills Germs that Cause:
- Plaque
- Gingivitis
- Bad breath
ADA Accepted
American Dental Association
- Helps reduce plaque
- Helps reduce gingivitis
Spring Mint
Made in the USA
with 90% OR MORE US PARTS
Factory Certified
1.5 LITERS (50.7 FL OZ)
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INGREDIENTS AND APPEARANCE
ANTISEPTIC MOUTHRINSE
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-072 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) SORBITOL (UNII: 506T60A25R) POLOXAMER 407 (UNII: TUF2IVW3M2) BENZOIC ACID (UNII: 8SKN0B0MIM) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM CITRATE (UNII: 1Q73Q2JULR) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-072-69 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/11/1989 2 NDC:49035-072-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/11/1989 3 NDC:49035-072-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/11/1989 4 NDC:49035-072-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/11/1989 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 11/11/1989 Labeler - Wal-Mart Stores, Inc. (051957769) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(49035-072) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(49035-072)