NDC11 43136060301
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 |
|---|---|
| 43136-0603-01 | 43136-0603 |
| 43136-0603-1 | 43136-0603 |
| 43136-603-01 | 43136-603 |
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 |
|---|---|---|---|---|---|---|
| PERIOE POP Complete Protection Prebiotic Mint Blast | SODIUM FLUORIDE | Tai Guk Pharm. Co., Ltd. | f547a468-d2fd-7176-e053-2995a90a5539 | 2025-01-01 | Warnings | 43136-603-01 43136-603 43136060301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.