Sun Pharmaceutical recalls AllerClear D-24 hr tablets due to failed moisture limits. This may cause reduced effectiveness or safety issues. Check your product for the NDC 63981-724-15 label.
Failed Moisture Limits
Sun Pharmaceutical is recalling Aller:Clear D-24 hr tablets because they failed moisture limits. This could mean the medication doesn't work as intended or poses safety risks. Affected products were sold between November 2022 and the current date.
The tablets failed moisture limits, which means they may not work properly or could become unsafe. This could lead to reduced effectiveness of the medication or potential safety issues if the tablets degrade over time.
People who own or use AllerClear D-24 hr tablets with the NDC 63981-724-15 label are affected. Those with allergies or respiratory conditions may be at higher risk due to potential reduced effectiveness.
Check for the NDC code 63981-724-15 on the blister pack. Products were manufactured by Ohm Laboratories Inc. in North Brunswick, NJ, starting November 2022.
Look for the NDC code 63981-724-15 on the blister pack to confirm if it's affected.
The product failed moisture limits, which could mean it doesn't work as intended or poses safety risks.
Check the product label for the NDC code 63981-724-15. If it matches, contact Sun Pharmaceutical for further instructions.
The recall is due to failed moisture limits, which may affect effectiveness but not pose a serious injury risk.
We’ve drafted a message you can send Sun Pharmaceutical Industries to request your refund or repair — edit it as you like.
Subject: Recall D-0069-2022 — Sun Pharmaceutical Industries Sun Pharmaceutical Industries Hello, I own a Sun Pharmaceutical Industries that is covered by recall D-0069-2022 from Sun Pharmaceutical Industries. 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.
