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.
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| HEB Extra Whitening | FLUORIDE | HEB | b76c3591-6383-4661-b3db-7a56b11202f7 | 2026-01-08 | Warnings | M022 |
| Crest Kids Advanced Color Changing | SODIUM MONOFLUOROPHOSPHATE | Procter & Gamble Manufactura, S de R.L. de C.V. | fc86b98e-d556-4769-e053-6394a90afc6e | 2026-01-08 | Warnings | M022 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.