Label: ANTISPETIC- eucalyptol, menthol, methyl salicylate, thymol mouthwash
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NDC Code(s):
59779-664-12,
59779-664-13,
59779-664-19,
59779-664-69, view more59779-664-77, 59779-664-86
- Packager: CVS Pharmacy, 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 April 18, 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
- Disclaimer
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SPL UNCLASSIFIED SECTION
Sealed with printed neckband for your protection. Do not use if broken or missing.
This product is not manufactured or distributed by Johnson & Johnson Corporation, distributor of Cool Mint Listerine Antiseptic Mouthwash.
Meets current TSA guidelines for carry-on luggage.
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsacket, RI 02895
(c) 2023 CVS Pharmacy, Inc.
CVS.com V-13687
1-800-SHOP-CVS
DSP-TN-21091
DSP-MO-20087
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principal display panel
CVS
Health
Compare to the active ingredints in Listerine Cool Mint Antiseptic*
Antiseptic
Mouthwash
ANTIGINGIVITIS/ANTIPLAQUE
Kills gemrs that cause plaque, gingivitis & bad breath
Blue Mint
ADA
Accepted
American
Dental
Association
- Helps prevent and reduce plaque
- Helps prevent and reduce gingivitis
3.2 FL OZ (94 mL)
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INGREDIENTS AND APPEARANCE
ANTISPETIC
eucalyptol, menthol, methyl salicylate, thymol mouthwashProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-664 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:59779-664-69 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/1992 2 NDC:59779-664-19 94 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/1992 3 NDC:59779-664-13 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/1992 4 NDC:59779-664-86 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/1992 5 NDC:59779-664-12 1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/1992 6 NDC:59779-664-77 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/15/1992 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 09/15/1992 Labeler - CVS Pharmacy, Inc (062312574) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(59779-664) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(59779-664)