NDC11 69396002102
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 |
|---|---|
| 69396-0021-02 | 69396-0021 |
| 69396-0021-2 | 69396-0021 |
| 69396-021-02 | 69396-021 |
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 |
|---|---|---|---|---|---|---|
| Zinc Oxide 20% | ZINC OXIDE | Trifecta Pharmaceuticals USA | 8cbe9b1f-fec0-9579-e053-2995a90ac461 | 2026-06-22 | Warnings | 69396-021 |
| Zinc Oxide 20% | ZINC OXIDE | Trifecta Pharmaceuticals USA | 63b551fc-7d16-c099-e053-2a91aa0a5f2c | 2026-05-18 | Warnings | 69396-021-02 69396-021 69396002102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.