Listerine Freshburst Intense Antiseptic Antigingivitis/Antiplaque Mouthwash
- Product NDC
- 69968-0956
- 11-digit product format
- 699680956
- Labeler code
- 69968
- Product ID
- 69968-0956_5d12e3b0-ed0d-477f-e063-6294a90a195c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Eucalyptol, Menthol, Methyl Salicylate, Thymol
- Dosage form
- MOUTHWASH
- Route
- ORAL
- Labeler
- Kenvue Brands LLC
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-01-23
- Substance
- METHYL SALICYLATE; THYMOL; EUCALYPTOL; MENTHOL
- Active strength
- .6; .64; .92; .42 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Listerine Freshburst Intense Antiseptic Antigingivitis/Antiplaque Mouthwash
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| METHYL SALICYLATE | .6 mg/mL |
| THYMOL | .64 mg/mL |
| EUCALYPTOL | .92 mg/mL |
| MENTHOL | .42 mg/mL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 69968-0956-1 | 69968095601 | 1000 mL in 1 BOTTLE (69968-0956-1) | 1000 ml | 2026-01-23 | No | No | Current |
| 69968-0956-2 | 69968095602 | 1500 mL in 1 BOTTLE (69968-0956-2) | 1500 ml | 2026-01-23 | No | No | Current |
| 69968-0956-3 | 69968095603 | 250 mL in 1 BOTTLE (69968-0956-3) | 250 ml | 2026-01-23 | No | No | Current |
| 69968-0956-5 | 69968095605 | 500 mL in 1 BOTTLE (69968-0956-5) | 500 ml | 2026-01-23 | No | No | Current |