Cobaltum Sulphuricum
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
- Cobaltum Sulphuricum
- Generic name
- COBALTUM SULPHURICUM
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f062baf5-af5d-8425-e053-2995a90a79cb
- SPL ID
- f062baf5-af5e-8425-e053-2995a90a79cb
- Version
- 1
- Effective date
- 2022-12-21
- Source export date
- 2026-09-28
- Source partition
- 9
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:02:27
| 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 | Cobaltum Sulphuricum | openfda.brand_name | |
| generic name | COBALTUM SULPHURICUM | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-2202-4 | openfda.package_ndc |
| ndc | package | 37662-2205-1 | openfda.package_ndc |
| ndc | package | 37662-2201-1 | openfda.package_ndc |
| ndc | package | 37662-2198-2 | openfda.package_ndc |
| ndc | package | 37662-2203-4 | openfda.package_ndc |
| ndc | package | 37662-2199-1 | openfda.package_ndc |
| ndc | package | 37662-2204-2 | openfda.package_ndc |
| ndc | package | 37662-2202-3 | openfda.package_ndc |
| ndc | package | 37662-2203-3 | openfda.package_ndc |
| ndc | package | 37662-2199-3 | openfda.package_ndc |
| ndc | package | 37662-2199-2 | openfda.package_ndc |
| ndc | package | 37662-2202-2 | openfda.package_ndc |
| ndc | package | 37662-2204-3 | openfda.package_ndc |
| ndc | package | 37662-2203-1 | openfda.package_ndc |
| ndc | package | 37662-2198-1 | openfda.package_ndc |
| ndc | package | 37662-2201-4 | openfda.package_ndc |
| ndc | package | 37662-2200-2 | openfda.package_ndc |
| ndc | package | 37662-2203-2 | openfda.package_ndc |
| ndc | package | 37662-2201-3 | openfda.package_ndc |
| ndc | package | 37662-2200-3 | openfda.package_ndc |
| ndc | package | 37662-2204-1 | openfda.package_ndc |
| ndc | package | 37662-2204-4 | openfda.package_ndc |
| ndc | package | 37662-2201-2 | openfda.package_ndc |
| ndc | package | 37662-2200-1 | openfda.package_ndc |
| ndc | package | 37662-2202-1 | openfda.package_ndc |
| ndc | package | 37662-2200-4 | openfda.package_ndc |
| ndc | package | 37662-2198-3 | openfda.package_ndc |
| ndc | product | 37662-2199 | openfda.product_ndc |
| ndc | product | 37662-2202 | openfda.product_ndc |
| ndc | product | 37662-2203 | openfda.product_ndc |
| ndc | product | 37662-2201 | openfda.product_ndc |
| ndc | product | 37662-2205 | openfda.product_ndc |
| ndc | product | 37662-2198 | openfda.product_ndc |
| ndc | product | 37662-2200 | openfda.product_ndc |
| ndc | product | 37662-2204 | openfda.product_ndc |
| ndc11 | package | 37662219903 | derived:openfda.package_ndc |
| ndc11 | package | 37662220301 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.