warnings
WARNINGS KEEP OUT OF REACH OF CHILDREN. FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.
Selenium Sulfide
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
- Selenium Sulfide
- Generic name
- SELENIUM SULFIDE
- Manufacturer
- Westminster Pharmaceuticals, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9fcab751-28f4-485a-aa37-169318a61110
- SPL ID
- 93f30d54-7096-4364-83df-65f94be0cafd
- Version
- 6
- Effective date
- 2025-04-23
- Source export date
- 2026-10-12
- 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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:11:10
| 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 | Selenium Sulfide | openfda.brand_name | |
| generic name | SELENIUM SULFIDE | openfda.generic_name | |
| manufacturer name | Westminster Pharmaceuticals, LLC | openfda.manufacturer_name | |
| ndc | package | 69367-229-18 | openfda.package_ndc |
| ndc | product | 69367-229 | openfda.product_ndc |
| ndc11 | package | 69367022918 | derived:openfda.package_ndc |
| rxcui | 706548 | openfda.rxcui | |
| spl id | 93f30d54-7096-4364-83df-65f94be0cafd | id | |
| spl set id | 9fcab751-28f4-485a-aa37-169318a61110 | set_id | |
| unii | Z69D9E381Q | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS In decreasing order of severity: skin irritation; occasional reports of increase in normal hair loss; discoloration of hair (can be avoided or minimized by thorough rinsing of hair after treatment). As with other shampoos, oiliness or dryness of hair and scalp may occur. To report a serious adverse event, please contact Westminster Pharmaceuticals at 1-844-221-7294 or call FDA at 1-800-FDA-1088 or fda.gov/medwatch.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.