Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
- NDC Code(s): 30142-664-12, 30142-664-19, 30142-664-77
- 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 March 15, 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
- SPL UNCLASSIFIED SECTION
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principal display panel
COMPARE to the active ingredients of COOL MINT LISTERINE*
SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION
Kroger
Blue Mint
ANTISEPTIC MOUTH RINSE
ANTIGINGIVITIS/ANTIPLAQUE
- Kills Germs That Cause Bad Breath, Plaque & the Gum Disease Gingivitis
- Meets Current TSA Guildlines For Carry-on Luggage
ADA AcceptedAmerica
Dental
Association
- Helps prevent and reduce plaque
- Helps prevent and reduce gingivitis
3.2 FL OZ (94 mL)
-
INGREDIENTS AND APPEARANCE
ANTISPETIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-664 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 BENZOATE (UNII: OJ245FE5EU) FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-664-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/05/1994 2 NDC:30142-664-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/05/1994 3 NDC:30142-664-19 94 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/05/1994 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 08/05/1994 Labeler - Kroger CO. (006999528) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(30142-664) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(30142-664)