warnings
Warnings Sore throat warning: if sore throat is severe, persists more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.
Sambucus Cold Flu Relief Elderberry
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 Cold Flu Relief Elderberry
- Generic name
- PELARGONIUM SIDOIDES ROOT, ACONITUM NAPELLUS, EUCALYPTUS GLOBULUS LEAF, SAMBUCUS NIGRA FLOWERING TOP, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, PHOSPHORUS, IPECAC
- Manufacturer
- Schwabe North America, Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5de8a3db-6103-4b69-8e47-c78bc7c6bfcd
- SPL ID
- f3b49948-0447-47f4-a07c-712c2e0c730c
- Version
- 1
- Effective date
- 2025-01-10
- Source export date
- 2026-10-12
- 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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:14:43
| 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 Cold Flu Relief Elderberry | openfda.brand_name | |
| generic name | PELARGONIUM SIDOIDES ROOT, ACONITUM NAPELLUS, EUCALYPTUS GLOBULUS LEAF, SAMBUCUS NIGRA FLOWERING TOP, BRYONIA ALBA ROOT, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, PHOSPHORUS, IPECAC | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc. | openfda.manufacturer_name | |
| ndc | package | 53499-5182-0 | openfda.package_ndc |
| ndc | product | 53499-5182 | openfda.product_ndc |
| ndc11 | package | 53499518200 | derived:openfda.package_ndc |
| spl id | f3b49948-0447-47f4-a07c-712c2e0c730c | id | |
| spl set id | 5de8a3db-6103-4b69-8e47-c78bc7c6bfcd | 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 | |
| unii | H6J53HEX8E | 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.