NDC11 65753010112
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 |
|---|---|
| 65753-0101-12 | 65753-0101 |
| 65753-101-12 | 65753-101 |
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 |
|---|---|---|---|---|---|---|
| CoreTex Sun X SPF 30 Thin | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE | CoreTex Products Inc | 980388b5-8314-3143-e053-2995a90a7288 | 2023-10-22 | Warnings | 65753-101-12 65753-101 65753010112 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.