NDC11 84573054712
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 |
|---|---|
| 84573-0547-12 | 84573-0547 |
| 84573-547-12 | 84573-547 |
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 Plus Topical Analgesic | MENTHOL | Real Time Products Inc. | fc509a55-594d-4d44-87db-33286e937581 | 2024-11-12 | Warnings | 84573-547-12 84573-547 84573054712 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.