warnings
Warning Sore Throat Warning: severe or persistent sore throat for more that 2 days or if accompanied by high fever, headache, nausea, vomiting or rash may be serious. Consult a physician promptly.
ALPHA CF
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
- ALPHA CF
- Generic name
- ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS
- Manufacturer
- Schwabe Mexico, S.A. de C.V.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 26afa426-eaae-437f-85a7-3bf0ad3d361b
- SPL ID
- 508e09f9-a43d-4cd5-9896-9c4eea845c8f
- Version
- 7
- Effective date
- 2022-05-03
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:07:27
| 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 | ALPHA CF | openfda.brand_name | |
| generic name | ACONITUM NAPELLUS, BRYONIA ALBA ROOT, EUCALYPTUS GLOBULUS LEAF, EUPATORIUM PERFOLIATUM FLOWERING TOP, GELSEMIUM SEMPERVIRENS ROOT, IPECAC, PHOSPHORUS | openfda.generic_name | |
| manufacturer name | Schwabe Mexico, S.A. de C.V. | openfda.manufacturer_name | |
| ndc | package | 68466-3398-4 | openfda.package_ndc |
| ndc | package | 68466-3398-1 | openfda.package_ndc |
| ndc | product | 68466-3398 | openfda.product_ndc |
| ndc11 | package | 68466339804 | derived:openfda.package_ndc |
| ndc11 | package | 68466339801 | derived:openfda.package_ndc |
| spl id | 508e09f9-a43d-4cd5-9896-9c4eea845c8f | id | |
| spl set id | 26afa426-eaae-437f-85a7-3bf0ad3d361b | 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 |
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.