Bismuthum Phosphoricum
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
- Bismuthum Phosphoricum
- Generic name
- BISMUTHUM PHOSPHORICUM
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- df26771d-0d68-dcbd-e053-2a95a90a8520
- SPL ID
- df26771d-0d69-dcbd-e053-2a95a90a8520
- Version
- 1
- Effective date
- 2022-05-16
- 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 06:02:15
| 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 | Bismuthum Phosphoricum | openfda.brand_name | |
| generic name | BISMUTHUM PHOSPHORICUM | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-0022-4 | openfda.package_ndc |
| ndc | package | 37662-0019-4 | openfda.package_ndc |
| ndc | package | 37662-0017-2 | openfda.package_ndc |
| ndc | package | 37662-0021-1 | openfda.package_ndc |
| ndc | package | 37662-0020-2 | openfda.package_ndc |
| ndc | package | 37662-0018-4 | openfda.package_ndc |
| ndc | package | 37662-0023-1 | openfda.package_ndc |
| ndc | package | 37662-0017-3 | openfda.package_ndc |
| ndc | package | 37662-0018-1 | openfda.package_ndc |
| ndc | package | 37662-0022-3 | openfda.package_ndc |
| ndc | package | 37662-0019-2 | openfda.package_ndc |
| ndc | package | 37662-0021-4 | openfda.package_ndc |
| ndc | package | 37662-0018-2 | openfda.package_ndc |
| ndc | package | 37662-0021-3 | openfda.package_ndc |
| ndc | package | 37662-0022-2 | openfda.package_ndc |
| ndc | package | 37662-0021-2 | openfda.package_ndc |
| ndc | package | 37662-0018-3 | openfda.package_ndc |
| ndc | package | 37662-0016-3 | openfda.package_ndc |
| ndc | package | 37662-0016-2 | openfda.package_ndc |
| ndc | package | 37662-0020-3 | openfda.package_ndc |
| ndc | package | 37662-0019-1 | openfda.package_ndc |
| ndc | package | 37662-0020-4 | openfda.package_ndc |
| ndc | package | 37662-0016-1 | openfda.package_ndc |
| ndc | package | 37662-0022-1 | openfda.package_ndc |
| ndc | package | 37662-0017-1 | openfda.package_ndc |
| ndc | package | 37662-0019-3 | openfda.package_ndc |
| ndc | package | 37662-0020-1 | openfda.package_ndc |
| ndc | product | 37662-0016 | openfda.product_ndc |
| ndc | product | 37662-0021 | openfda.product_ndc |
| ndc | product | 37662-0020 | openfda.product_ndc |
| ndc | product | 37662-0019 | openfda.product_ndc |
| ndc | product | 37662-0022 | openfda.product_ndc |
| ndc | product | 37662-0017 | openfda.product_ndc |
| ndc | product | 37662-0018 | openfda.product_ndc |
| ndc | product | 37662-0023 | openfda.product_ndc |
| ndc11 | package | 37662002201 | derived:openfda.package_ndc |
| ndc11 | package | 37662002103 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.