Pharmaceutical Associates recalls 16 fl oz guaifenesin-codeine oral solution due to superpotent sodium benzoate preservative. This may cause serious health risks. Consumers should contact the company for details.
Superpotent; sodium benzoate preservative
Pharmaceutical Associates is recalling guaifenesin and codeine phosphate oral solution bottles that contain a superpotent sodium benzoate preservative. This could pose serious health risks to users, especially those with sensitive systems.
The sodium benzoate preservative in this product is described as superpotent, which could lead to serious health issues. The exact mechanism is not specified in the recall notice.
People who own or use the recalled guaifenesin-codeine oral solution bottles are affected. Those with sensitive health conditions may be at higher risk.
Look for bottles labeled 'Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml)' from Pharmaceutical Associates. The lot number is 4B07 with an expiration date of October 31, 2026.
Identify the product by checking the label for the specific formulation and lot number.
The recall states the product contains a superpotent sodium benzoate preservative, which may pose serious health risks. The official notice does not confirm if it is safe to use.
The recall record does not mention any remedy or replacement options.
The recall record does not specify a remedy, so the official notice does not provide instructions on what to do.
We’ve drafted a message you can send Pharmaceutical Associates to request your refund or repair — edit it as you like.
Subject: Recall D-0222-2025 — Pharmaceutical Associates Pharmaceutical Associates Hello, I own a Pharmaceutical Associates that is covered by recall D-0222-2025 from Pharmaceutical Associates. 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.
