NDC11 72344011603
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 |
|---|---|
| 72344-0116-03 | 72344-0116 |
| 72344-0116-3 | 72344-0116 |
| 72344-116-03 | 72344-116 |
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 |
|---|---|---|---|---|---|---|
| SURFACE SUN SPF 50 DRY TOUCH Fragrance Free | HOMOSALATE 10.00% OCTOCRYLENE 6.00% AVOBENZONE 3.00% | Surface Products Corp | 65f52fc8-8ddb-4282-9bc0-92a7d0e0c0f2 | 2026-05-05 | Warnings | 72344-116-03 72344-116 72344011603 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.