NDC11 84573051712
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 |
|---|---|
| 84573-0517-12 | 84573-0517 |
| 84573-517-12 | 84573-517 |
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 |
|---|---|---|---|---|---|---|
| Real Time Pain Relief Maxx Topical Analgesic | MENTHOL | REAL TIME PRODUCTS, INC | f45eb95a-2813-4124-bdb0-54e078a8237d | 2024-08-20 | Warnings | 84573-517-12 84573-517 84573051712 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.