NDC11 69256003509
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 |
|---|---|
| 69256-0035-09 | 69256-0035 |
| 69256-0035-9 | 69256-0035 |
| 69256-035-09 | 69256-035 |
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 |
|---|---|---|---|---|---|---|
| Salicylic Acid | WART REMOVER LIQUID | Harris Teeter, LLC | d53756d4-6739-48da-b367-84531f989170 | 2025-10-07 | Warnings | 69256-035-09 69256-035 69256003509 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.