NDC11 75568004300
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 |
|---|---|
| 75568-0043-0 | 75568-0043 |
| 75568-0043-00 | 75568-0043 |
| 75568-043-00 | 75568-043 |
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 |
|---|---|---|---|---|---|---|
| BonicaEaseX Menthol Pain Relieving | MENTHOL, UNSPECIFIED FORM | Planet (Anhui) Pharmaceutical Co.,Ltd | 4d84b4fb-8f55-4b2b-b261-858edb7f3144 | 2026-04-10 | Warnings | 75568-043-00 75568-043 75568004300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.