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
- 869735c4-f8d6-1b5b-e053-2a91aa0a5920
- SPL ID
- f67ce46f-fe86-e06f-e053-2a95a90ae28d
- Version
- 2
- Effective date
- 2023-03-09
- Source export date
- 2026-09-28
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:14:07
| 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 | 0220-4830-41 | openfda.package_ndc |
| ndc | product | 0220-4830 | openfda.product_ndc |
| ndc11 | package | 00220483041 | derived:openfda.package_ndc |
| spl id | f67ce46f-fe86-e06f-e053-2a95a90ae28d | id | |
| spl set id | 869735c4-f8d6-1b5b-e053-2a91aa0a5920 | set_id | |
| unii | 70FD1KFU70 | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.