NDC 69968-0790-02 - Listerine Gum Therapy Glacier Mint
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
- 69968-0790
- Requested NDC
- 69968-0790-02
- Package NDCs from labels
- 69968-0790-5, 69968-0790-1, 69968-0790-9, 69968-0790-2, 69968-0790-3, 69968-0790-02
- 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 Gum Therapy Glacier Mint - 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 |
|---|---|---|---|---|---|---|
| 69968-0790-1 | Listerine Gum TherapyGlacier Mint | 1000 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1000 | 6 | |
| 69968-0790-2 | Listerine Gum TherapyGlacier Mint | 1500 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1500 | 6 | |
| 69968-0790-3 | Listerine Gum TherapyGlacier Mint | 2 in 1 TRAY | MOUTHWASH | 2 | 6 | |
| 69968-0790-3 | Listerine Gum TherapyGlacier Mint | 1500 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 1500 | 6 | |
| 69968-0790-5 | Listerine Gum TherapyGlacier Mint | 500 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 500 | 6 | |
| 69968-0790-9 | Listerine Gum TherapyGlacier Mint | 95 mL in 1 BOTTLE, PLASTIC | MOUTHWASH | 95 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69968-0790 | LISTERINE GUM THERAPY GLACIER MINT (EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL) MOUTHWASH [KENVUE BRANDS LLC] | 6 | Current NDC, 6 package rows | 20241114_ed6889b6-58db-41cf-e053-2a95a90a7de2.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.