NDC 69968-0949-09 - Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 69968-0949
- Requested NDC
- 69968-0949-09
- Package NDCs from labels
- 69968-0949-1, 69968-0949-8, 69968-0949-3, 69968-0949-2, 69968-0949-5, 69968-0949-9, 69968-0949-09
- Manufacturer
- Kenvue Brands LLC
- Effective date
- 2025-12-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Eucalyptol, Menthol, Methyl Salicylate, Thymol - Kenvue Brands LLC | Kenvue Brands LLC | 2025-12-02 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69968-0949-1 | Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | 1000 mL in 1 BOTTLE | MOUTHWASH | 1000 | 1 | |
| 69968-0949-2 | Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | 1500 mL in 1 BOTTLE | MOUTHWASH | 1500 | 1 | |
| 69968-0949-3 | Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | 250 mL in 1 BOTTLE | MOUTHWASH | 250 | 1 | |
| 69968-0949-5 | Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | 500 mL in 1 BOTTLE | MOUTHWASH | 500 | 1 | |
| 69968-0949-8 | Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | 1500 mL in 1 BOTTLE | MOUTHWASH | 1500 | 1 | |
| 69968-0949-8 | Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | 2 in 1 TRAY | MOUTHWASH | 2 | 1 | |
| 69968-0949-9 | Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash | 95 mL in 1 BOTTLE | MOUTHWASH | 95 | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.