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
- 2026-10-30
- 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/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:56:18
| 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.