Natrum 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
- Natrum Sulphuricum
- Generic name
- NATRUM SULPHURICUM
- Manufacturer
- Hahnemann Laboratories, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- ed024be8-873e-7ad6-e053-2995a90a3c84
- SPL ID
- ed024be8-873f-7ad6-e053-2995a90a3c84
- Version
- 1
- Effective date
- 2022-11-08
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:23:28
| 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 | Natrum Sulphuricum | openfda.brand_name | |
| generic name | NATRUM SULPHURICUM | openfda.generic_name | |
| manufacturer name | Hahnemann Laboratories, INC. | openfda.manufacturer_name | |
| ndc | package | 37662-1895-2 | openfda.package_ndc |
| ndc | package | 37662-1901-2 | openfda.package_ndc |
| ndc | package | 37662-1899-3 | openfda.package_ndc |
| ndc | package | 37662-1902-2 | openfda.package_ndc |
| ndc | package | 37662-1903-1 | openfda.package_ndc |
| ndc | package | 37662-1901-3 | openfda.package_ndc |
| ndc | package | 37662-1902-1 | openfda.package_ndc |
| ndc | package | 37662-1900-2 | openfda.package_ndc |
| ndc | package | 37662-1900-4 | openfda.package_ndc |
| ndc | package | 37662-1896-1 | openfda.package_ndc |
| ndc | package | 37662-1902-4 | openfda.package_ndc |
| ndc | package | 37662-1896-3 | openfda.package_ndc |
| ndc | package | 37662-1897-1 | openfda.package_ndc |
| ndc | package | 37662-1896-2 | openfda.package_ndc |
| ndc | package | 37662-1900-1 | openfda.package_ndc |
| ndc | package | 37662-1901-4 | openfda.package_ndc |
| ndc | package | 37662-1897-2 | openfda.package_ndc |
| ndc | package | 37662-1899-1 | openfda.package_ndc |
| ndc | package | 37662-1900-3 | openfda.package_ndc |
| ndc | package | 37662-1897-3 | openfda.package_ndc |
| ndc | package | 37662-1899-2 | openfda.package_ndc |
| ndc | package | 37662-1899-4 | openfda.package_ndc |
| ndc | package | 37662-1895-3 | openfda.package_ndc |
| ndc | package | 37662-1898-1 | openfda.package_ndc |
| ndc | package | 37662-1901-1 | openfda.package_ndc |
| ndc | package | 37662-1898-4 | openfda.package_ndc |
| ndc | package | 37662-1897-4 | openfda.package_ndc |
| ndc | package | 37662-1898-2 | openfda.package_ndc |
| ndc | package | 37662-1898-3 | openfda.package_ndc |
| ndc | package | 37662-1895-1 | openfda.package_ndc |
| ndc | package | 37662-1902-3 | openfda.package_ndc |
| ndc | product | 37662-1903 | openfda.product_ndc |
| ndc | product | 37662-1899 | openfda.product_ndc |
| ndc | product | 37662-1902 | openfda.product_ndc |
| ndc | product | 37662-1896 | openfda.product_ndc |
| ndc | product | 37662-1895 | openfda.product_ndc |
| ndc | product | 37662-1900 | openfda.product_ndc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.