NDC11 65753010939
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 |
|---|---|
| 65753-0109-39 | 65753-0109 |
| 65753-109-39 | 65753-109 |
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 Professional Outdoor Skin Protection Wallet | CORETEX PROFESSIONAL OUTDOOR SKIN PROTECTION WALLET | CoreTex Products Inc | f57bc089-405b-cdcd-e053-2995a90a9d12 | 2025-10-09 | Warnings | 65753-109-39 65753010939 |
| CoreTex Sun X SPF 30 Multipack New | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | CoreTex Products | f4ed9d7f-2d03-87d1-e053-2a95a90a3b4f | 2023-10-22 | Warnings | 65753-109 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.