NDC11 70518323300
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 |
|---|---|
| 70518-3233-0 | 70518-3233 |
| 70518-3233-00 | 70518-3233 |
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 |
|---|---|---|---|---|---|---|
| TRETINOIN | TRETINOIN | REMEDYREPACK INC. | c4d5155b-046d-4f94-bafc-651b572c2bd5 | 2026-04-07 | Warnings, Adverse reactions | 70518-3233-0 70518-3233 70518323300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.