McKesson Drug Company recalls Erythromycin Topical Gel USP 2% 60g tubes (NDC 63739-053-68) manufactured by Teligent Pharma due to discontinued stability testing. Products were distributed with a June 2022 expiration date.
CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc.is discontinuing its stability study program.
McKesson Drug Company is recalling Erythromycin Topical Gel USP 2% 60g tubes because the manufacturer stopped its stability testing program. This recall affects prescription-only products with a June 2022 expiration date.
The manufacturer discontinued its stability testing program, which means the product's long-term safety and effectiveness could be compromised. However, the recall does not indicate immediate harm to users.
Prescription holders of Erythromycin Topical Gel USP 2% 60g tubes with NDC 63739-053-68. Patients who have the product with a June 2022 expiration date are most at risk.
Check for the product name 'Erythromycin Topical Gel USP 2%', 60g tube size, NDC code 63739-053-68, and expiration date of June 30, 2022.
Verify the product's NDC code (63739-053-68) and expiration date (June 30, 2022) to confirm it is affected.
The recall is due to the manufacturer discontinuing stability testing, but the product is not expected to cause immediate harm. Consult your healthcare provider for advice.
Check for the NDC code 63739-053-68 and expiration date of June 30, 2022 on the product label.
The recall does not specify a remedy, so contact McKesson Drug Company for guidance on next steps.
We’ve drafted a message you can send McKesson Drug Company to request your refund or repair — edit it as you like.
Subject: Recall D-0851-2022 — McKesson Drug Company McKesson Drug Company Hello, I own a McKesson Drug Company that is covered by recall D-0851-2022 from McKesson Drug Company. 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.
