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
- 8695c4fb-437f-91c2-e053-2a91aa0a4e71
- SPL ID
- 003abd8e-d4e1-fc69-e063-6394a90a381f
- Version
- 2
- Effective date
- 2023-07-11
- Source export date
- 2026-11-06
- 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/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:00:21
| 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 | 0220-4817-41 | openfda.package_ndc |
| ndc | product | 0220-4817 | openfda.product_ndc |
| ndc11 | package | 00220481741 | derived:openfda.package_ndc |
| spl id | 003abd8e-d4e1-fc69-e063-6394a90a381f | id | |
| spl set id | 8695c4fb-437f-91c2-e053-2a91aa0a4e71 | set_id | |
| unii | 70FD1KFU70 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.