sodium sulfacetamide and sulfur
Generic: sodium sulfacetamide and sulfur
Labeler: westminster pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
sodium sulfacetamide and sulfur
Generic Name
sodium sulfacetamide and sulfur
Labeler
westminster pharmaceuticals, llc
Dosage Form
SUSPENSION
Routes
Active Ingredients
sulfacetamide sodium 80 mg/mL, sulfur 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
69367-245
Product ID
69367-245_b4e89e57-397a-4578-bc59-709cb46db033
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2021-06-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69367245
Hyphenated Format
69367-245
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
sodium sulfacetamide and sulfur (source: ndc)
Generic Name
sodium sulfacetamide and sulfur (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/mL
- 40 mg/mL
Packaging
- 473 mL in 1 BOTTLE (69367-245-16)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "b4e89e57-397a-4578-bc59-709cb46db033", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["1010234"], "spl_set_id": ["e9b60d3f-3f3f-477d-92d7-fe0ba07e21de"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (69367-245-16)", "package_ndc": "69367-245-16", "marketing_start_date": "20210618"}], "brand_name": "Sodium Sulfacetamide and Sulfur", "product_id": "69367-245_b4e89e57-397a-4578-bc59-709cb46db033", "dosage_form": "SUSPENSION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "69367-245", "generic_name": "Sodium Sulfacetamide and Sulfur", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Sulfacetamide and Sulfur", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "80 mg/mL"}, {"name": "SULFUR", "strength": "40 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210618", "listing_expiration_date": "20261231"}