NDC11 49035070001
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 |
|---|---|
| 49035-0700-01 | 49035-0700 |
| 49035-0700-1 | 49035-0700 |
| 49035-700-01 | 49035-700 |
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 |
|---|---|---|---|---|---|---|
| Equate Pain Relieving Ultra Strength | CAMPHOR, MENTHOL, METHYL SALICYLATE | Wal-Mart Stores Inc | 5ed1d7b3-925e-4a18-8e15-636f5b442ad7 | 2026-01-19 | Warnings | 49035-700-01 49035-700 49035070001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.