NDC11 79073001703
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 |
|---|---|
| 79073-0017-03 | 79073-0017 |
| 79073-0017-3 | 79073-0017 |
| 79073-017-03 | 79073-017 |
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 |
|---|---|---|---|---|---|---|
| natouch | SALICYLIC ACID | Natouch LLC | 4cb2cc1b-1793-b0c4-e063-6294a90a430f | 2026-03-08 | Warnings | 79073-017-03 79073-017 79073001703 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.