NDC11 24208049015
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 |
|---|---|
| 24208-0490-15 | 24208-0490 |
| 24208-490-15 | 24208-490 |
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 |
|---|---|---|---|---|---|---|
| Soothe XP | LIGHT MINERAL OIL AND MINERAL OIL | Bausch & Lomb Incorporated | c0f053da-8d22-433e-a36e-79cf15ad387f | 2024-09-20 | Warnings | 24208-490-15 24208-490 24208049015 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.