NDC11 49404030201
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 |
|---|---|
| 49404-0302-01 | 49404-0302 |
| 49404-0302-1 | 49404-0302 |
| 49404-302-01 | 49404-302 |
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 |
|---|---|---|---|---|---|---|
| Dr.Jart Premium Beauty Balm Light Medium-Medium | ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE | Have & Be Co., Ltd. | 02a87c6b-3c7d-5942-e063-6294a90aa452 | 2025-02-06 | Warnings | 49404-302-01 49404-302 49404030201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.