Listerine FreshBurst Antiseptic Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash — NDC 69968-0239-8 (Billing 69968-0239-08)
This is a package of Listerine FreshBurst Antiseptic Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash from Kenvue Brands LLC, no longer marketed (first marketed Aug 2018), no longer in the FDA NDC Directory.
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 1043619
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
Clinical
Listerine FreshBurst is an over-the-counter antiseptic mouthwash that contains four active ingredients: eucalyptol, menthol, methyl salicylate, and thymol. These compounds are typically used in oral rinse products for their antimicrobial properties and are commonly included to help reduce bacteria in the mouth. This product is marketed under FDA's monograph rules for mouthwashes rather than through an individual product application.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 1, 2026
Ask a licensed pharmacist directly — free, answered by our team.
Pricing
A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.
| Price system | Per each | Per package |
|---|---|---|
| Retail pharmacies payNADAC · weekly | Not in the retail survey — common for institutional, discontinued, or low-volume packs. | |
| Medicaid paysCMS SDUD · 12 mo | No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data. | |
| Medicare drug plans payPart D · quarterly | No Part D plan price is available for this NDC in our data. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 2, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 69968-0239-01 69968-0239-1 Main listing | 1000 mL in 1 BOTTLE, PLASTIC | 2018-09-18 | — | Active |
| 69968-0239-02 69968-0239-2 | 250 mL in 1 BOTTLE, PLASTIC | 2019-05-03 | — | Active |
| 69968-0239-03 69968-0239-3 | 1500 mL in 1 BOTTLE, PLASTIC | 2018-08-28 | — | Active |
| 69968-0239-05 69968-0239-5 | 500 mL in 1 BOTTLE, PLASTIC | 2018-08-17 | — | Active |
| 69968-0239-08 You're viewing this | 2 BOTTLE, PLASTIC in 1 PACKAGE / 1500 mL in 1 BOTTLE, PLASTIC | 2020-04-24 | — | Discontinued by firm |
Pack size FAQ
What quantity is in this package?
What NDC number is used to bill for this package of Listerine FreshBurst Antiseptic Eucalyptol, MENTHOL, UNSPECIFIED FORM, Methyl Salicylate, and Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash?
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Sep 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Sep 3, 2026
Inactive Ingredients / Excipients
Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
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UNII 3K9958V90M
A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
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UNII 8SKN0B0MIM
Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
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UNII 35SW5USQ3G
A synthetic yellow dye used to color medicines. It helps make tablets, capsules, and liquids visually distinct so patients can easily identify their medication.
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UNII 3P3ONR6O1S
A synthetic green dye approved by the FDA for use in medicines and foods. It serves as a colorant to make the pill or liquid visually distinctive and help with product identification.
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UNII TUF2IVW3M2
Poloxamer 407 is a synthetic polymer made from ethylene oxide and propylene oxide. In medicines, it acts as a thickener, emulsifier, and solubilizer to help mix ingredients and create the right texture.
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UNII SB8ZUX40TY
Saccharin sodium is an artificial sweetener made from saccharin salt. It's added to medicines to improve taste, especially in liquid formulations for children or bitter drugs.
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UNII OJ245FE5EU
Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
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UNII 506T60A25R
Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
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UNII 059QF0KO0R
Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
9 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.- FDA label on DailyMed · label index refreshed Oct 1, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses helps prevent and reduce: plaque gingivitis
⏱️ Dosage and Administration ▾
Directions rinse full strength for 30 seconds with 20 mL (2/3 fluid ounce or 4 teaspoonfuls) morning and night do not swallow
⚠️ Warnings ▾
Warnings Do not use in children under 12 years of age Ask a dentist if symptoms persist Ask a dentist if symptoms persist , new symptoms appear, or conditions worsen after regular use Keep out of reach of children. Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
📦 Storage and Handling ▾
Other information this rinse is not intended to replace brushing or flossing store at room temperature cold weather may cloud this product. Its antiseptic properties are not affected.
🧪 Active Ingredient ▾
Active ingredients Purposes Eucalyptol (0.092%) Antiplaque/antigingivitis Menthol (0.042%) Antiplaque/antigingivitis Methyl Salicylate (0.060%) Antiplaque/antigingivitis Thymol (0.064%) Antiplaque/antigingivitis
🧪 Inactive Ingredients ▾
Inactive ingredients Water, Alcohol (21.6% v/v), Sorbitol, Poloxamer 407, Benzoic Acid, Sodium Saccharin, Flavor, Sodium Benzoate, Yellow 10, Green 3
🎯 Purpose ▾
Active ingredients Purposes Eucalyptol (0.092%) Antiplaque/antigingivitis Menthol (0.042%) Antiplaque/antigingivitis Methyl Salicylate (0.060%) Antiplaque/antigingivitis Thymol (0.064%) Antiplaque/antigingivitis
📄 Do Not Use ▾
Do not use in children under 12 years of age
📄 Ask a Doctor Before Use If ▾
Ask a dentist if symptoms persist Ask a dentist if symptoms persist , new symptoms appear, or conditions worsen after regular use
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions? call toll-free 888-222-0182 or 215-273-8755 (collect)
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL - 1500 mL Bottle Label ANTISEPTIC LISTERINE ® FRESHBURST ® FOR A FRESHER & CLEANER MOUTH THAN BRUSHING ALONE ADA Accepted American Dental Association ®
1.5L (1 Qt 1 Pt 2.7 fl oz) Listerine_001
About this NDC listing & data coverage
What data is (and isn’t) available for this NDC — tap to expand
| NDC identity (package / product / labeler codes) | ✓ Available |
| Labeler | ✓ Available |
| Product & package description | ✓ Available |
| Marketing category & status | ✓ Available |
| Active ingredient / dosage form / route | ✓ Available |
| FDA label (SPL via DailyMed) | ✓ Available |
| Package photos | ✓ Available |
| Inactive ingredients (structured) | ✓ Available |
| NADAC pharmacy acquisition price (CMS) | — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey. |
| Orange Book / therapeutic-equivalence data | — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope. |
| HCPCS J-code billing crosswalk | — Not published for this NDC Most self-administered / retail products have no J-code — that is normal. |
| Medicaid utilization (CMS SDUD) | — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold. |