NDC11 72957000601
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 |
|---|---|
| 72957-0006-01 | 72957-0006 |
| 72957-0006-1 | 72957-0006 |
| 72957-006-01 | 72957-006 |
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 |
|---|---|---|---|---|---|---|
| HA Physical Tint SPF 44 | ZINC OXIDE, TITANIUM DIOXIDE | Private Label Skin Care | a5e19d77-703e-41e0-9a02-19227dc6c819 | 2025-02-27 | Warnings | 72957-006-01 72957-006 72957000601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.