NDC 44523-560
Sulfacetamide Sodium, Sulfur 50 mg per 1 g / 100 mg per 1 g emulsion
On the label: Biocomp Pharma, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Medical Products Laboratories, Inc. | Philadelphia, PA, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 13, 2023 · 8 inspections |
Product details
- Generic drug
- Sulfacetamide and Sulfur: every company that makes it
- Form
- emulsion, topical
- Strength
- 50 mg per 1 g / 100 mg per 1 g
- Approval
- unapproved drug other
- On the market since
- Sep 15, 2011
- Package NDCs
44523-560-0644523-560-0844523-560-12- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
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