NDC11 49527007401
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 |
|---|---|
| 49527-0074-01 | 49527-0074 |
| 49527-0074-1 | 49527-0074 |
| 49527-074-01 | 49527-074 |
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 |
|---|---|---|---|---|---|---|
| MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25 | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, AND ZINC OXIDE | CLINIQUE LABORATORIES LLC | 159410d4-4479-4442-b371-bde72aae3e1e | 2023-10-13 | Warnings | 49527-074-01 49527-074 49527007401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.