JB Chemicals recalls 10mg cetirizine tablets with incorrect labeling that may cause confusion about the product's identity.
Tablet/Capsules Imprinted with Wrong ID
JB Chemicals is recalling 10mg cetirizine hydrochloride tablets that have incorrect labeling. This could lead to confusion about which medication is being taken, potentially causing the wrong drug to be used.
The tablets have incorrect labeling that may cause confusion about which medication is being taken. This could lead to the wrong drug being used, especially if someone is allergic to cetirizine or similar antihistamines.
People who purchased the recalled 10mg cetirizine tablets from the listed distributors in the US. Those with allergies to cetirizine or similar antihistamines are at higher risk.
Look for bottles labeled 'Cetirizine Hydrochloride Tablets USP 10 mg, 500 Tablets' with NDC 16571-402-50 and lot numbers PY925014 or PY925013. These were distributed by Rising Pharma Holdings in the US.
Verify the product label for the correct NDC number and lot numbers.
No, this recall is for labeling issues that could cause confusion, not a safety hazard.
Check for NDC 16571-402-50 and lot numbers PY925014 or PY925013 on the bottle.
Check the label to confirm the product. If you have the correct label, no action is needed.
We’ve drafted a message you can send JB Chemicals to request your refund or repair — edit it as you like.
Subject: Recall D-0033-2026 — JB Chemicals JB Chemicals Hello, I own a JB Chemicals that is covered by recall D-0033-2026 from JB Chemicals. 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.
