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
- 86989825-e2f9-3d46-e053-2991aa0a7e28
- SPL ID
- 0a3400ec-70d0-340c-e063-6394a90ad39d
- Version
- 2
- Effective date
- 2023-11-15
- Source export date
- 2026-10-30
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:33:20
| 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 | 0220-4827-41 | openfda.package_ndc |
| ndc | product | 0220-4827 | openfda.product_ndc |
| ndc11 | package | 00220482741 | derived:openfda.package_ndc |
| spl id | 0a3400ec-70d0-340c-e063-6394a90ad39d | id | |
| spl set id | 86989825-e2f9-3d46-e053-2991aa0a7e28 | set_id | |
| unii | 70FD1KFU70 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.