warnings
Warnings Sore throat warning: if sore throat is severe, persists more than 2 days, is accompanied or following by a fever, headache, rash, nausea, or vomiting, c onsult a doctor promptly.
Umcka FastActives Berry
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
- Umcka FastActives Berry
- Generic name
- PELARGONIUM SIDOIDES, ACONITUM NAPELLUS, BRYONIA, EUCALYPTUS GLOBULUS, EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, IPECACUANHA, PHOSPHORUS
- Manufacturer
- Schwabe North America, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 149941fb-9b5f-42f2-bf0c-e5980f7daad6
- SPL ID
- ce73b91f-d303-4b7a-98eb-31ca9bca585d
- Version
- 9
- Effective date
- 2024-10-23
- 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 05:56:48
| 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 | Umcka FastActives Berry | openfda.brand_name | |
| generic name | PELARGONIUM SIDOIDES, ACONITUM NAPELLUS, BRYONIA, EUCALYPTUS GLOBULUS, EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, IPECACUANHA, PHOSPHORUS | openfda.generic_name | |
| manufacturer name | Schwabe North America, Inc | openfda.manufacturer_name | |
| ndc | package | 53499-9349-0 | openfda.package_ndc |
| ndc | product | 53499-9349 | openfda.product_ndc |
| ndc11 | package | 53499934900 | derived:openfda.package_ndc |
| spl id | ce73b91f-d303-4b7a-98eb-31ca9bca585d | id | |
| spl set id | 149941fb-9b5f-42f2-bf0c-e5980f7daad6 | set_id | |
| unii | 27YLU75U4W | openfda.unii | |
| unii | 639KR60Q1Q | openfda.unii | |
| unii | 62I3C8233L | openfda.unii | |
| unii | T7J046YI2B | openfda.unii | |
| unii | U0NQ8555JD | 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.