A&D Original Ointment, Diaper Rash O:16 oz jars recalled due to improper storage conditions. Consumers should check labels for NDC 11523-0096-3.
CGMP Deviations: products were stored outside the drug label specifications.
A&D Original Ointment and Diaper Rash Ointment jars are being recalled because they were stored outside drug label specifications. This could lead to safety issues if the product is used improperly.
The ointment was stored outside the required drug label specifications, which could affect its safety and effectiveness. This storage issue might lead to improper use or reduced product quality.
Parents and caregivers who use A&D diaper rash ointment for infants are most at risk. The product is sold in 16-ounce jars with NDC 11521-0096-3.
Check for the 16-ounce jar labeled with NDC 11523-0096-3. The product is sold by Bayer Healthcare Pharmaceutica under the A&D brand.
Look for the NDC code 11523-0096-3 on the jar to confirm it is recalled.
The recall is due to storage issues, not safety risks. However, it is recommended to check the label before use.
Check for the 16-ounce jar with NDC 11523-0096-3 on the label.
The recall does not specify a remedy, so check the label and contact the manufacturer if unsure.
We’ve drafted a message you can send A&D to request your refund or repair — edit it as you like.
Subject: Recall D-1322-2022 — A&D A&D Hello, I own a A&D that is covered by recall D-1322-2022 from A&D. 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.
