Quick answers
- What is Exelderm?
- Exelderm is a brand name of Sulconazole nitrate, a prescription medicine. The FDA NDC Directory lists 2 Exelderm products in 2 strengths and forms.
- Who makes Exelderm?
- Journey holds the FDA application for Exelderm (NDA018738, approved August 30, 1985).
- Is there a generic or store brand of Exelderm?
- Yes. The FDA NDC Directory lists 2 other products with the same active ingredients, strength and form as a Exelderm product. Ask your pharmacist whether one is right for you.
- Has Exelderm been recalled?
- No recall linked to Exelderm products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Exelderm is
Each Exelderm product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Sulconazole nitrate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| sulconazole nitrate 1% cream (topical) | Exelderm | 1 product, 1 company | DailyMed |
| sulconazole nitrate 10 mg/mL solution (topical) | Exelderm | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Sulconazole nitrate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
Companies that list Exelderm
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Exelderm products.
- Journey Medical Corporation2 products
Recalls
No recall linked to Exelderm products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.