Quick answers
- What is Ala-Scalp?
- Ala-Scalp is a brand name of Hydrocortisone, a prescription medicine. The FDA NDC Directory lists 1 Ala-Scalp product in 1 strength and form.
- Who makes Ala-Scalp?
- Legacy holds the FDA application for Ala-Scalp (ANDA083231, approved February 28, 1973).
- Is there a generic or store brand of Ala-Scalp?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Ala-Scalp product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Ala-Scalp been recalled?
- No recall linked to Ala-Scalp products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Ala-Scalp is
Each Ala-Scalp 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.
Hydrocortisone · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| hydrocortisone 20 mg/mL lotion (topical) | Ala-Scalp | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Hydrocortisone →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA083231 | Legacy | February 28, 1973 | 1 |
Companies that list Ala-Scalp
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Ala-Scalp products.
- Derm Ventures LLC1 product
Recalls
No recall linked to Ala-Scalp 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.