CoValence Laboratories recalls hydrocortisone 1% Remedy Gel due to subpotent drug levels. Affected products have specific NDC and lot numbers. Consumers should contact the distributor for details.
Subpotent Drug
CoValence Laboratories is recalling hydrocortisone 1% Remedy Gel because it may contain insufficient active ingredient. This could lead to ineffective treatment for skin conditions. The recall affects specific product batches with known NDC and lot numbers.
The product may have subpotent hydrocortisone levels, meaning it contains less active ingredient than labeled. This could result in the gel not working properly for skin conditions. However, the risk is not severe enough to cause serious injury.
People who purchased the Remedy Gel from glo Skin Beauty in Denver, CO, between the dates of distribution. Those with skin conditions requiring hydrocortisone treatment are most at risk.
Check for NDC numbers 66915-531-12 or 66915-531-13, and lot numbers 4155D2 or 4155D3. The product expires May 15, 2026, and was distributed by glo Skin Beauty in Denver, CO.
Look for NDC numbers 66915-531-12 or 66915-531-13 and lot numbers 4155D2 or 4155D3 on the label.
The product may have subpotent hydrocortisone levels, but it is not unsafe to use. The recall is for potential ineffectiveness, not immediate harm.
Check for NDC numbers 66915-531-12 or 66915-531-13 and lot numbers 4155D2 or 4155D3 on the label.
The recall does not specify a remedy, so contact glo Skin Beauty in Denver, CO for further instructions.
We’ve drafted a message you can send CoValence Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-0480-2026 — CoValence Laboratories CoValence Laboratories Hello, I own a CoValence Laboratories that is covered by recall D-0480-2026 from CoValence Laboratories. 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.
