NDC11 49967006901
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 |
|---|---|
| 49967-0069-01 | 49967-0069 |
| 49967-0069-1 | 49967-0069 |
| 49967-069-01 | 49967-069 |
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 |
|---|---|---|---|---|---|---|
| Kiehls Since 1851 Dermatologist Solutions AutoTone Discoloration and UV Solution Broad Spectrum SPF 30 Sunscreen | AVOBENZONE, HOMOSALATE, OCTISALATE AND OCTOCRYLENE | L'Oreal USA Products Inc | 6dbbc8ce-9457-4405-bb38-aa0c7550c62c | 2024-06-27 | Warnings | 49967-069-01 49967-069 49967006901 |