Sodium Sulfacetamide 9.8% and Sulfur 4.8% Cleanser
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 9.8% and Sulfur 4.8% Cleanser
- Generic name
- SULFACETAMIDE SODIUM, SULFUR
- Manufacturer
- KMM Pharmaceuticals, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- db857027-0175-e452-e053-2995a90a4df5
- SPL ID
- db857027-0176-e452-e053-2995a90a4df5
- Version
- 1
- Effective date
- 2022-03-31
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:51
| 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 9.8% and Sulfur 4.8% Cleanser | openfda.brand_name | |
| generic name | SULFACETAMIDE SODIUM, SULFUR | openfda.generic_name | |
| manufacturer name | KMM Pharmaceuticals, LLC | openfda.manufacturer_name | |
| ndc | package | 52187-546-10 | openfda.package_ndc |
| ndc | product | 52187-546 | openfda.product_ndc |
| ndc11 | package | 52187054610 | derived:openfda.package_ndc |
| rxcui | 1494169 | openfda.rxcui | |
| spl id | db857027-0176-e452-e053-2995a90a4df5 | id | |
| spl set id | db857027-0175-e452-e053-2995a90a4df5 | set_id | |
| unii | 4NRT660KJQ | openfda.unii | |
| unii | 70FD1KFU70 | 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.