Sodium Sulfacetamide
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
- Sodium Sulfacetamide
- Generic name
- SODIUM SULFACETAMIDE
- Manufacturer
- BioComp Pharma, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- ac7863c6-387c-4c90-bfaa-5f1544e1e887
- SPL ID
- 462cce62-a759-da87-e063-6394a90a3ed4
- Version
- 6
- Effective date
- 2025-12-17
- 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 05:25:37
| Harmonized routes |
|---|
| TOPICAL |
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 | Sodium Sulfacetamide | openfda.brand_name | |
| generic name | SODIUM SULFACETAMIDE | openfda.generic_name | |
| manufacturer name | BioComp Pharma, Inc. | openfda.manufacturer_name | |
| ndc | package | 44523-510-08 | openfda.package_ndc |
| ndc | product | 44523-510 | openfda.product_ndc |
| ndc11 | package | 44523051008 | derived:openfda.package_ndc |
| rxcui | 832864 | openfda.rxcui | |
| spl id | 462cce62-a759-da87-e063-6394a90a3ed4 | id | |
| spl set id | ac7863c6-387c-4c90-bfaa-5f1544e1e887 | set_id | |
| unii | 4NRT660KJQ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS: Sulfonamides are known to cause Stevens-Johnson syndrome in hypersensitive individuals. Stevens-Johnson syndrome also has been reported following the use of sodium sulfacetamide topically. Cases of drug-induced systemic lupus erythematosus from topical sulfacetamide also have been reported. In one of these cases, there was a fatal outcome. KEEP OUT OF THE REACH OF CHILDREN.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS: Reports of irritation and hypersensitivity to sodium sulfacetamide are uncommon. The following adverse reactions, reported after administration of sterile ophthalmic sodium sulfacetamide, are noteworthy: instances of Stevens-Johnson syndrome and instances of local hypersensitivity which progressed to a syndrome resembling systemic lupus erythematosus; in one case a fatal outcome was reported (see WARNINGS).
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.