NDC11 73002023101
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 |
|---|---|
| 73002-0231-01 | 73002-0231 |
| 73002-0231-1 | 73002-0231 |
| 73002-231-01 | 73002-231 |
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 73002-231 | 73002-231-01 | D | Discontinued by firm | 2026-10-05 |
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 |
|---|---|---|---|---|---|---|
| PAIN RELIEF SNAKE VENOM AND HEMP | COBRA VENOM (NAJA NAJA) 4X, HEMP EXTRACT (CANNABIS SATIVA) 2X, MOCCASIN VENOM (A.PISCIVORUS) 6X | Green Earth Health Inc. | 64305797-5890-40e6-bbfc-dfdc1cedffee | 2025-07-22 | Warnings | 73002-231-01 73002-231 73002023101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.