NDC11 84130000150
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 |
|---|---|
| 84130-0001-50 | 84130-0001 |
| 84130-001-50 | 84130-001 |
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 |
|---|---|---|---|---|---|---|
| Sun Shield Body Glow SPF50 | HOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE | Koco Life LLC | 180aa4d5-6dac-e658-e063-6394a90a3287 | 2024-06-28 | Warnings | 84130-001-50 84130-001 84130000150 |
| Sun Essentials SPF Duo Kit | AVOBENZONE, HOMOSALATE, OCTOCRYLENE, OCTISALATE | Koco Life LLC | 1c329b86-664e-de1f-e063-6394a90a7c23 | 2024-06-28 | Warnings | 84130-001-50 84130000150 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.