NDC11 69968079301
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 69968-0793-01 | 69968-0793 |
| 69968-0793-1 | 69968-0793 |
| 69968-793-01 | 69968-793 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Tylenol Precise Cooling Pain Relieving | LIDOCAINE, MENTHOL | Kenvue Brands LLC | fc0a3404-b174-3952-e053-6294a90a1e02 | 2026-02-16 | Warnings | 69968-0793-1 69968-0793 69968079301 |
| TYLENOL Extra Strength / TYLENOL Precise Cooling Pain Relief | ACETAMINOPHEN, LIDOCAINE, MENTHOL | Kenvue Brands LLC | 2611e984-0dd5-bda1-e063-6394a90a559a | 2024-11-26 | Warnings | 69968-0793-1 69968079301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.