Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 63941-001-12, 63941-001-69, 63941-001-77, 63941-001-86
- Packager: Valu Merchandisers Co.
- 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 January 27, 2023
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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
- Questions?
- Disclaimer
- Adverse Reactions
-
Principal display panel
Best Choice
Sealed With Printed Neckband For Your Protection
COMPARE TO THE ACTIVE INGREDIENTS IN LISTERINE*
SPRING MINT
Mouth Rinse
ANTISEPTIC
ANTIGINGIVITIS/ANTIPLAQUE
ADA
Accepted
American Dental Association
- Helps reduce plaque
- Helps reduce gingivitis
Kills Germs That Cause Bad Breath, Plaque & Gingivitis Gum Diseae
1L (33.8 FL OZ)
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INGREDIENTS AND APPEARANCE
ANTISPETIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63941-001 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:63941-001-69 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/09/1995 2 NDC:63941-001-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/09/1995 3 NDC:63941-001-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/09/1995 4 NDC:63941-001-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/09/1995 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 06/09/1995 Labeler - Valu Merchandisers Co. (868703513) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(63941-001) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(63941-001)