NDC 69968-0239-01 - Listerine FreshBurst Antiseptic
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
- 69968-0239
- Requested NDC
- 69968-0239-01
- Package NDCs from labels
- 69968-0239-5, 69968-0239-2, 69968-0239-1, 69968-0239-3, 69968-0239-8, 69968-0239-01
- Manufacturer
- Kenvue Brands LLC
- Effective date
- 2024-11-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Listerine FreshBurst Antiseptic - Kenvue Brands LLC | Kenvue Brands LLC | 2024-11-11 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69968-0239-1 | Listerine FreshBurst Antiseptic | 1000 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1000 | 9 | |
| 69968-0239-2 | Listerine FreshBurst Antiseptic | 250 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 250 | 9 | |
| 69968-0239-3 | Listerine FreshBurst Antiseptic | 1500 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1500 | 9 | |
| 69968-0239-5 | Listerine FreshBurst Antiseptic | 500 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 500 | 9 | |
| 69968-0239-8 | Listerine FreshBurst Antiseptic | 2 in 1 PACKAGE | MOUTHWASH | 2 | 9 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69968-0239 | LISTERINE FRESHBURST ANTISEPTIC (EUCALYPTOL, MENTHOL, UNSPECIFIED FORM, METHYL SALICYLATE, AND THYMOL) MOUTHWASH [KENVUE BRANDS LLC] | 9 | Current NDC, Legacy NDC, 5 package rows | 20241114_62b5c3ee-01cc-4c4e-9f28-e7dafa7372d8.zip |
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.