sulfacetamide sodium and sulfur sodium sulfacetamide - sulfur
Generic: sulfacetamide sodium and sulfur
Labeler: allegis pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
sulfacetamide sodium and sulfur sodium sulfacetamide - sulfur
Generic Name
sulfacetamide sodium and sulfur
Labeler
allegis pharmaceuticals, llc
Dosage Form
SUSPENSION
Routes
Active Ingredients
sulfacetamide sodium 90 mg/mL, sulfur 42.5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
28595-501
Product ID
28595-501_4a912755-c660-18d3-e063-6294a90a1a38
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2027-12-31
Marketing Start
2024-06-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
28595501
Hyphenated Format
28595-501
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
sulfacetamide sodium and sulfur sodium sulfacetamide - sulfur (source: ndc)
Generic Name
sulfacetamide sodium and sulfur (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 90 mg/mL
- 42.5 mg/mL
Packaging
- 237 mL in 1 BOTTLE (28595-501-08)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4a912755-c660-18d3-e063-6294a90a1a38", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["2531383"], "spl_set_id": ["1aa1025f-c568-34d3-e063-6394a90a37b8"], "manufacturer_name": ["Allegis Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (28595-501-08)", "package_ndc": "28595-501-08", "marketing_start_date": "20240618"}], "brand_name": "sulfacetamide sodium and sulfur Sodium Sulfacetamide - Sulfur", "product_id": "28595-501_4a912755-c660-18d3-e063-6294a90a1a38", "dosage_form": "SUSPENSION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "28595-501", "generic_name": "sulfacetamide sodium and sulfur", "labeler_name": "Allegis Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "sulfacetamide sodium and sulfur", "brand_name_suffix": "Sodium Sulfacetamide - Sulfur", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "90 mg/mL"}, {"name": "SULFUR", "strength": "42.5 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240618", "listing_expiration_date": "20271231"}