NDC11 73251001000
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 |
|---|---|
| 73251-0010-0 | 73251-0010 |
| 73251-0010-00 | 73251-0010 |
| 73251-010-00 | 73251-010 |
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 73251-010 | 73251-010-00 | D | Discontinued by firm | 2026-08-11 |
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 |
|---|---|---|---|---|---|---|
| Purito Sunday Adventure Sunscreen SPF 50, 50 mL | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | Hinature | bf16f535-97fc-4fd8-9310-8b6bbc82baae | 2026-03-31 | Warnings | 73251-010-00 73251-010 73251001000 |