NDC11 71630014715
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 |
|---|---|
| 71630-0147-15 | 71630-0147 |
| 71630-147-15 | 71630-147 |
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 |
|---|---|---|---|---|---|---|
| doTERRA sun Face Daily Moisturizer | ZINC OXIDE | doTERRA International, LLC | f3836517-e3ec-5e9e-e053-2a95a90a7af1 | 2025-01-28 | Warnings | 71630-147-15 71630-147 71630014715 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.