CoValence Laboratories recalls Skin Rehab Calming Skin Gel and Hydrocortisone Balm due to subpotent drug levels. Affected products have specific NDC and expiration dates. Consumers should contact the manufacturer for details.
Subpotent Drug
CoValence Laboratories is recalling Skin Rehab Calming Skin Gel and Hydrocortisone Balm products because they contain subpotent hydrocortisone. This means the medication may not be as effective as intended, potentially leading to inadequate treatment of skin conditions.
The product contains subpotent hydrocortisone, meaning the medication concentration is lower than intended. This could result in the product being less effective for treating skin inflammation or other conditions. However, it does not pose a direct risk of injury or harm.
People who own or use the recalled Skin Rehab Calming Skin Gel or Hydrocortisone Balm products. Those with skin conditions requiring hydrocortisone treatment may be most affected.
Check for the product name 'Skin Rehab Calming Skin Gel' or 'Hydrocortisone Balm' with NDC 66915-531-04 and expiration date 07/03/2026. The products were distributed by A.C.E. Inc. near DFW International Airport.
Identify the product by checking the NDC code 66915-531-04 and expiration date 07/03/2026.
The product may be less effective than intended due to subpotent hydrocortisone, but it does not pose a direct risk of injury or harm.
Check for the NDC code 66915-531-04 and expiration date 07/03/2026 on the product label.
The recall does not specify a remedy, so contact CoValence Laboratories 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-0481-2026 — CoValence Laboratories CoValence Laboratories Hello, I own a CoValence Laboratories that is covered by recall D-0481-2026 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.
