NDC11 49527022201
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 |
|---|---|
| 49527-0222-01 | 49527-0222 |
| 49527-0222-1 | 49527-0222 |
| 49527-222-01 | 49527-222 |
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 |
|---|---|---|---|---|---|---|
| DRAMATICALLY DIFFERENT MOISTURIZING LTN BROAD SPECTRUM SPF35 | AVOBENZONE,HOMOSALATE,OCTISALATE,OCTOCRYLENE | CLINIQUE LABORATORIES LLC | 316bf6f8-7d30-2560-e063-6294a90afb8a | 2026-01-15 | Warnings | 49527-222-01 49527-222 49527022201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.