warnings
WARNINGS Stop use and ask a physician if symptoms persist for more than 3 days or worsen.
Nux vomica 30C - 3-Pack
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Nux vomica 30C - 3-Pack
- Generic name
- NUX VOMICA
- Manufacturer
- SEVENE USA
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 31f0db61-0d7e-6fe5-e063-6394a90abc58
- SPL ID
- 352c320f-ca9a-4f50-e063-6394a90a5a14
- Version
- 2
- Effective date
- 2025-05-15
- Source export date
- 2026-09-28
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:19:14
| Harmonized routes |
|---|
| SUBLINGUAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Nux vomica 30C - 3-Pack | openfda.brand_name | |
| generic name | NUX VOMICA | openfda.generic_name | |
| manufacturer name | SEVENE USA | openfda.manufacturer_name | |
| ndc | package | 76472-5004-1 | openfda.package_ndc |
| ndc | package | 76472-5004-2 | openfda.package_ndc |
| ndc | product | 76472-5004 | openfda.product_ndc |
| ndc11 | package | 76472500401 | derived:openfda.package_ndc |
| ndc11 | package | 76472500402 | derived:openfda.package_ndc |
| spl id | 352c320f-ca9a-4f50-e063-6394a90a5a14 | id | |
| spl set id | 31f0db61-0d7e-6fe5-e063-6394a90abc58 | set_id | |
| unii | 269XH13919 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.