warnings
Warnings Sore throat warning: if sore throat is severe, persists more than 2 days, is accompanied or followed by a fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
Sambucus Flu Relief
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
- Sambucus Flu Relief
- Generic name
- ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS, SAMBUCUS NIGRA FLOWERING TOP
- Manufacturer
- Schwabe North America, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ca7d57b0-ffae-415f-a959-b0c88ae7dd40
- SPL ID
- e952da08-d4e8-46a8-8330-99accec78283
- Version
- 4
- Effective date
- 2025-12-08
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:56:44
| 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 | Sambucus Flu Relief | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS, SAMBUCUS NIGRA FLOWERING TOP | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc. | openfda.manufacturer_name | |
| ndc | package | 53499-0803-5 | openfda.package_ndc |
| ndc | product | 53499-0803 | openfda.product_ndc |
| ndc11 | package | 53499080305 | derived:openfda.package_ndc |
| spl id | e952da08-d4e8-46a8-8330-99accec78283 | id | |
| spl set id | ca7d57b0-ffae-415f-a959-b0c88ae7dd40 | set_id | |
| unii | 27YLU75U4W | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | 62I3C8233L | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | U0NQ8555JD | openfda.unii | |
| unii | CT03BSA18U | openfda.unii | |
| unii | 1W0775VX6E | openfda.unii | |
| unii | S546YLW6E6 | 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.