Ecometics recalls Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment due to CGMP deviations. Products with lot numbers 1E346A (exp Nov 2023) and 2E304A (exp Oct 2024) may be unsafe.
CGMP DEVIATIONS
Ecometics is recalling Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment because of manufacturing quality control issues. This could mean the product doesn't meet safety standards and might pose risks if used improperly.
CGMP deviations refer to manufacturing quality control failures. This means the product may not meet safety standards, potentially causing harm if used incorrectly or in sensitive skin areas.
People who own or use Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment with lot numbers 1E346A (expiring November 2023) or 2E304A (expiring October 2024) are affected. Those using the ointment for pain relief or minor cuts may be at risk.
Check the metal tube packaging for lot numbers 1E346A (expires November 2023) or 2E304A (expires October 2024). The ointment contains camphor, phenol, tannic acid, and oxide.
Look for lot numbers 1E346A (expiring November 2023) or 2E304A (expiring October 2024) on the metal tube packaging.
The hazard is CGMP deviations, which means manufacturing quality control issues that could affect safety standards.
Check the metal tube packaging for lot numbers 1E346A (expires November 2023) or 2E304A (expires October 2024).
The recall record does not specify a remedy, so contact Ecometics directly for guidance.
We’ve drafted a message you can send Ecometics to request your refund or repair — edit it as you like.
Subject: Recall D-0452-2023 — Ecometics Ecometics Hello, I own a Ecometics that is covered by recall D-0452-2023 from Ecometics. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.