Beryllium 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
- Beryllium Sulphuricum
- Generic name
- BERYLLIUM SULPHURICUM
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- df2509a8-ba0c-e1b9-e053-2a95a90af056
- SPL ID
- df2509a8-ba0d-e1b9-e053-2a95a90af056
- Version
- 1
- Effective date
- 2022-05-16
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:43:22
| 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 | Beryllium Sulphuricum | openfda.brand_name | |
| generic name | BERYLLIUM SULPHURICUM | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-0009-2 | openfda.package_ndc |
| ndc | package | 37662-0009-3 | openfda.package_ndc |
| ndc | package | 37662-0011-1 | openfda.package_ndc |
| ndc | package | 37662-0015-1 | openfda.package_ndc |
| ndc | package | 37662-0013-1 | openfda.package_ndc |
| ndc | package | 37662-0011-2 | openfda.package_ndc |
| ndc | package | 37662-0008-1 | openfda.package_ndc |
| ndc | package | 37662-0013-3 | openfda.package_ndc |
| ndc | package | 37662-0010-2 | openfda.package_ndc |
| ndc | package | 37662-0011-3 | openfda.package_ndc |
| ndc | package | 37662-0010-3 | openfda.package_ndc |
| ndc | package | 37662-0014-4 | openfda.package_ndc |
| ndc | package | 37662-0013-4 | openfda.package_ndc |
| ndc | package | 37662-0009-1 | openfda.package_ndc |
| ndc | package | 37662-0014-3 | openfda.package_ndc |
| ndc | package | 37662-0008-2 | openfda.package_ndc |
| ndc | package | 37662-0012-3 | openfda.package_ndc |
| ndc | package | 37662-0014-1 | openfda.package_ndc |
| ndc | package | 37662-0012-4 | openfda.package_ndc |
| ndc | package | 37662-0012-2 | openfda.package_ndc |
| ndc | package | 37662-0011-4 | openfda.package_ndc |
| ndc | package | 37662-0008-3 | openfda.package_ndc |
| ndc | package | 37662-0010-1 | openfda.package_ndc |
| ndc | package | 37662-0014-2 | openfda.package_ndc |
| ndc | package | 37662-0010-4 | openfda.package_ndc |
| ndc | package | 37662-0013-2 | openfda.package_ndc |
| ndc | package | 37662-0012-1 | openfda.package_ndc |
| ndc | product | 37662-0014 | openfda.product_ndc |
| ndc | product | 37662-0010 | openfda.product_ndc |
| ndc | product | 37662-0011 | openfda.product_ndc |
| ndc | product | 37662-0015 | openfda.product_ndc |
| ndc | product | 37662-0013 | openfda.product_ndc |
| ndc | product | 37662-0012 | openfda.product_ndc |
| ndc | product | 37662-0008 | openfda.product_ndc |
| ndc | product | 37662-0009 | openfda.product_ndc |
| ndc11 | package | 37662000803 | derived:openfda.package_ndc |
| ndc11 | package | 37662001404 | derived:openfda.package_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.