warnings
WARNING If you are pregnant or nursing, ask a health care professional before using this product. Keep this product out of the reach of children.
Lumavex
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
- Lumavex
- Generic name
- MULTIVITAMIN
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 4139742d-d091-121c-e063-6394a90a6221
- SPL ID
- 4139742d-d090-121c-e063-6394a90a6221
- Version
- 1
- Effective date
- 2025-10-15
- Source export date
- 2026-09-28
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:27:58
| Harmonized routes |
|---|
| ORAL |
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 | Lumavex | openfda.brand_name | |
| generic name | MULTIVITAMIN | openfda.generic_name | |
| manufacturer name | Oncora Pharma, LLC | openfda.manufacturer_name | |
| ndc | package | 85477-610-30 | openfda.package_ndc |
| ndc | product | 85477-610 | openfda.product_ndc |
| ndc11 | package | 85477061030 | derived:openfda.package_ndc |
| spl id | 4139742d-d090-121c-e063-6394a90a6221 | id | |
| spl set id | 4139742d-d091-121c-e063-6394a90a6221 | set_id | |
| unii | BR1SN1JS2W | openfda.unii | |
| unii | 19F5HK2737 | openfda.unii | |
| unii | 25X51I8RD4 | openfda.unii | |
| unii | TLM2976OFR | openfda.unii | |
| unii | 935E97BOY8 | openfda.unii | |
| unii | PQ6CK8PD0R | openfda.unii | |
| unii | M572600E5P | openfda.unii | |
| unii | 68Y4CF58BV | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Call your doctor about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.