NDC11 76348097103
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 |
|---|---|
| 76348-0971-03 | 76348-0971 |
| 76348-0971-3 | 76348-0971 |
| 76348-971-03 | 76348-971 |
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 |
|---|---|---|---|---|---|---|
| MG PLUS ROLL ON | MENTHOL ROLL ON | RENU LABORATORIES, LLC | 535dc42f-38c7-2afc-e063-6294a90ae23d | 2026-06-03 | Warnings | 76348-971-03 76348-971 76348097103 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.