Viona Pharmaceuticals recalls Dapsone Gel 7.5% (60g pump) due to crystallization risk. This prescription medication may cause issues if stored improperly. Check NDC 72578-094-02 and lot T400512 for affected units.
Crystallization
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% (60g pump) because crystallization could cause problems. This is a prescription-only medication that may need special handling to avoid issues.
Crystallization in the gel could lead to changes in the medication's properties. This might affect how the drug works or causes issues if the product is not stored properly.
Prescription patients using Dapsone Gel 7.5% (60g pump) with NDC 72578-094-02 and lot number T400512 are affected. Patients with this specific medication are most at risk.
Check for the NDC code 72578-094-02 and lot number T400512 on the product label. This Dapsone Gel 7.5% (60g pump) is only available through prescription.
Look for NDC 72578-094-02 and lot number T400512 on the label.
The recall does not specify safety concerns, so it's best to check with your doctor or pharmacist.
The recall record does not provide a remedy, so contact Viona Pharmaceuticals for guidance.
Check the NDC code 72578-094-02 and lot number T400512 on the product label.
We’ve drafted a message you can send Viona Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0011-2025 — Viona Pharmaceuticals Viona Pharmaceuticals Hello, I own a Viona Pharmaceuticals that is covered by recall D-0011-2025 from Viona Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
