sulfacetamide sodium, sulfur
Generic: sulfacetamide sodium, sulfur
Labeler: bantry pharma, llcDrug Facts
Product Profile
Brand Name
sulfacetamide sodium, sulfur
Generic Name
sulfacetamide sodium, sulfur
Labeler
bantry pharma, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
sulfacetamide sodium 100 mg/mL, sulfur 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
81542-202
Product ID
81542-202_36c18a52-2828-aaa0-e063-6294a90a6ce1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2023-02-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81542202
Hyphenated Format
81542-202
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, sulfur (source: ndc)
Generic Name
sulfacetamide sodium, sulfur (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
- 50 mg/mL
Packaging
- 355 mL in 1 BOTTLE (81542-202-12)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "36c18a52-2828-aaa0-e063-6294a90a6ce1", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["999613"], "spl_set_id": ["f433db67-d8a6-320e-e053-2995a90aab52"], "manufacturer_name": ["Bantry Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "355 mL in 1 BOTTLE (81542-202-12)", "package_ndc": "81542-202-12", "marketing_start_date": "20230208"}], "brand_name": "SULFACETAMIDE SODIUM, SULFUR", "product_id": "81542-202_36c18a52-2828-aaa0-e063-6294a90a6ce1", "dosage_form": "SOLUTION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "81542-202", "generic_name": "SULFACETAMIDE SODIUM, SULFUR", "labeler_name": "Bantry Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SULFACETAMIDE SODIUM, SULFUR", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "100 mg/mL"}, {"name": "SULFUR", "strength": "50 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20230208", "listing_expiration_date": "20261231"}