NDC11 65753010122
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 |
|---|---|
| 65753-0101-22 | 65753-0101 |
| 65753-101-22 | 65753-101 |
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 65753-101 | 65753-101-22 | D | Discontinued by firm | 2026-08-03 |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated 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 | 65753-101-22 65753-101 65753010122 |