NDC11 83810001206
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 |
|---|---|
| 83810-0012-06 | 83810-0012 |
| 83810-0012-6 | 83810-0012 |
| 83810-012-06 | 83810-012 |
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 |
|---|---|---|---|---|---|---|
| Broad Spectrum SPF 50 sunscreen | HOMOSALATE 10%, OCTISALATE 5.0%, AVOBENZONE 3.0% | Florida Squeezed | 34ffc25c-16e3-4c7c-9d46-9d9f279c074b | 2025-08-26 | Warnings | 83810-012-06 83810-012 83810001206 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.