Bismuthum Subnitricum
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 Subnitricum
- Generic name
- BISMUTHUM SUBNITRICUM
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- de0f84f3-5f89-2ac2-e053-2995a90a8caa
- SPL ID
- de0f84f3-5f8a-2ac2-e053-2995a90a8caa
- Version
- 1
- Effective date
- 2022-05-02
- Source export date
- 2026-10-12
- 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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:37:55
| 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 |
|---|---|---|---|
| ndc11 | package | 63545049404 | derived:openfda.package_ndc |
| ndc11 | package | 63545049703 | derived:openfda.package_ndc |
| ndc11 | package | 63545049603 | derived:openfda.package_ndc |
| ndc11 | package | 63545049203 | derived:openfda.package_ndc |
| ndc11 | package | 63545049701 | derived:openfda.package_ndc |
| ndc11 | package | 63545049504 | derived:openfda.package_ndc |
| ndc11 | package | 63545049602 | derived:openfda.package_ndc |
| ndc11 | package | 63545049103 | derived:openfda.package_ndc |
| ndc11 | package | 63545049403 | derived:openfda.package_ndc |
| ndc11 | package | 63545049304 | derived:openfda.package_ndc |
| ndc11 | package | 63545049601 | derived:openfda.package_ndc |
| ndc11 | package | 63545049201 | derived:openfda.package_ndc |
| ndc11 | package | 63545049402 | derived:openfda.package_ndc |
| ndc11 | package | 63545049401 | derived:openfda.package_ndc |
| ndc11 | package | 63545049302 | derived:openfda.package_ndc |
| ndc11 | package | 63545049101 | derived:openfda.package_ndc |
| ndc11 | package | 63545049704 | derived:openfda.package_ndc |
| ndc11 | package | 63545049801 | derived:openfda.package_ndc |
| ndc11 | package | 63545049202 | derived:openfda.package_ndc |
| ndc11 | package | 63545049303 | derived:openfda.package_ndc |
| ndc11 | package | 63545049301 | derived:openfda.package_ndc |
| ndc11 | package | 63545049102 | derived:openfda.package_ndc |
| ndc11 | package | 63545049702 | derived:openfda.package_ndc |
| ndc11 | package | 63545049503 | derived:openfda.package_ndc |
| ndc11 | package | 63545049502 | derived:openfda.package_ndc |
| spl id | de0f84f3-5f8a-2ac2-e053-2995a90a8caa | id | |
| spl set id | de0f84f3-5f89-2ac2-e053-2995a90a8caa | set_id | |
| unii | H19J064BA5 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.