Sulphur
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
- Sulphur
- Generic name
- SULFUR
- Manufacturer
- Boiron
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e205d5d0-7c2b-11e6-87a0-424c58303031
- SPL ID
- 0a33e170-e8ae-25a8-e063-6394a90addf5
- Version
- 4
- Effective date
- 2023-11-15
- Source export date
- 2026-10-27
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 21:05:37
| 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 | Sulphur | openfda.brand_name | |
| generic name | SULFUR | openfda.generic_name | |
| manufacturer name | Boiron | openfda.manufacturer_name | |
| ndc | package | 0220-4823-41 | openfda.package_ndc |
| ndc | product | 0220-4823 | openfda.product_ndc |
| ndc11 | package | 00220482341 | derived:openfda.package_ndc |
| spl id | 0a33e170-e8ae-25a8-e063-6394a90addf5 | id | |
| spl set id | e205d5d0-7c2b-11e6-87a0-424c58303031 | set_id | |
| unii | 70FD1KFU70 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.