sodium sulfacetamide 8% and sulfur 4%

Generic: sulfacetamide sodium, sulfur

Labeler: akron pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name sodium sulfacetamide 8% and sulfur 4%
Generic Name sulfacetamide sodium, sulfur
Labeler akron pharma inc.
Dosage Form SUSPENSION
Routes
TOPICAL
Active Ingredients

sulfacetamide sodium 80 mg/mL, sulfur 40 mg/mL

Manufacturer
Akron Pharma Inc.

Identifiers & Regulatory

Product NDC 71399-0487
Product ID 71399-0487_a4bb29b0-065f-428b-9d9b-bb4e564449d3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2024-09-13

Pharmacologic Class

Classes
sulfonamide antibacterial [epc] sulfonamides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713990487
Hyphenated Format 71399-0487

Supplemental Identifiers

RxCUI
1010234
UNII
4NRT660KJQ 70FD1KFU70

Packaging Origin

Original Packager
true

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 8% and sulfur 4% (source: ndc)
Generic Name sulfacetamide sodium, sulfur (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/mL
  • 40 mg/mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE, PLASTIC (71399-0487-6)
source: ndc

Packages (1)

Ingredients (2)

sulfacetamide sodium (80 mg/mL) sulfur (40 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "a4bb29b0-065f-428b-9d9b-bb4e564449d3", "openfda": {"unii": ["4NRT660KJQ", "70FD1KFU70"], "rxcui": ["1010234"], "spl_set_id": ["bfbe625c-5679-4363-913a-2ab03198f4f0"], "manufacturer_name": ["Akron Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (71399-0487-6)", "package_ndc": "71399-0487-6", "marketing_start_date": "20240913"}], "brand_name": "Sodium Sulfacetamide 8% and Sulfur 4%", "product_id": "71399-0487_a4bb29b0-065f-428b-9d9b-bb4e564449d3", "dosage_form": "SUSPENSION", "pharm_class": ["Sulfonamide Antibacterial [EPC]", "Sulfonamides [CS]"], "product_ndc": "71399-0487", "generic_name": "SULFACETAMIDE SODIUM, SULFUR", "labeler_name": "Akron Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Sulfacetamide 8% and Sulfur 4%", "active_ingredients": [{"name": "SULFACETAMIDE SODIUM", "strength": "80 mg/mL"}, {"name": "SULFUR", "strength": "40 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240913", "listing_expiration_date": "20261231"}