Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.
Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send G & W Laboratories, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0636-2017 — G & W Laboratories, Inc. G & W Laboratories, Inc. recalls Ciclopirox Olamine Cream USP, 0.77%, pa Hello, I own a G & W Laboratories, Inc. recalls Ciclopirox Olamine Cream USP, 0.77%, packaged in a) 15 g tubes (NDC 0713-0638-15), b) 30 g tubes (NDC 0713-0638-31), that is covered by recall D-0636-2017 from G & W Laboratories, Inc.. 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.
