NDC11 43136052260
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 |
|---|---|
| 43136-0522-60 | 43136-0522 |
| 43136-522-60 | 43136-522 |
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 |
|---|---|---|---|---|---|---|
| POP Gel Whatzzup Watermelon | SODIUM FLUORIDE | Tai Guk Pharm. Co., Ltd. | 05b18bb6-9fbf-469b-e063-6294a90a4f2f | 2025-01-01 | Warnings | 43136-522-60 43136-522 43136052260 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.