A-S Medication Solutions recalls 10mg cetirizine tablets due to incorrect labeling showing 90 tablets when only 30 were actually in the box. This may cause confusion about dosage.
Labeling: Not Elsewhere classified: Product was relabeled as 90 tablet count product although it was a manufacturer in a box with 30 tablet count tablets.
A-S Medication Solutions is recalling 10mg cetirizine hydrochloride tablets that were labeled as 90-count but actually contain only 30 tablets. This labeling error could lead to incorrect dosing if users assume there are more tablets than actually present.
The product was labeled as a 90-tablet count bottle, but it actually contains only 30 tablets. This labeling error could lead to users taking more medication than intended if they miscount the tablets.
People who own or use the recalled 10mg cetirizine tablets (90-count bottle) from A-S Medication Solutions. Those most at risk are individuals who may miscount tablets due to the labeling error.
Check for the 10mg cetirizine hydrochloride tablets in a 90-count bottle with the manufacturer's address in Libertyville, IL. The product was distributed by A-S Medication Solutions with NDC code 50090-5510-3.
Verify the product label shows 90 tablets, but the actual contents contain only 30 tablets.
No, this is a labeling error that could cause confusion about the number of tablets, but it does not pose a safety risk.
Look for the 10mg cetirizine hydrochloride tablets in a 90-count bottle with the NDC code 50090-5510-3, distributed by A-S Medication Solutions.
The recall does not require immediate action, but you should check the label to confirm the tablet count and contact the manufacturer if you have concerns.
We’ve drafted a message you can send A-S Medication Solutions to request your refund or repair — edit it as you like.
Subject: Recall D-0096-2022 — A-S Medication Solutions A-S Medication Solutions Hello, I own a A-S Medication Solutions that is covered by recall D-0096-2022 from A-S Medication Solutions. 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.
