NDC11 10893053102
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 |
|---|---|
| 10893-0531-02 | 10893-0531 |
| 10893-0531-2 | 10893-0531 |
| 10893-531-02 | 10893-531 |
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 |
|---|---|---|---|---|---|---|
| Naturasil Mite B Gone TREATMENT Kit | SULFUR, THUJA OCCIDENTALIS | Nature's Innovation, Inc. | 21ddffb1-6d71-4460-a79c-90e2d65a2bd3 | 2024-02-07 | Warnings | 10893-531-02 10893-531 10893053102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.