Neilmed Pharmaceuticals recalls SinuFrin nasal decongestant due to sub-potent drug content. Affected units have NDC 13709-325-01. Consumers should check product details and contact the company for guidance.
Sub-potent Drug
Neilmed Pharmaceuticals is recalling SinuFrin nasal decongestant because it contains less active ingredient than labeled. This could lead to reduced effectiveness, but the recall does not indicate a risk of serious injury or harm.
The product contains a sub-potent drug, meaning it has less active ingredient than advertised. This could result in the decongestant being less effective than expected. However, the recall does not mention any risk of serious injury or harm.
People who own or use the SinuFrin nasal decongestant with NDC 13709-325-01 are affected. Those most at risk are individuals relying on the product for nasal congestion relief.
Check for the NDC code 13709-325-01 on the product label. The product was manufactured by Neilmed Pharmaceuticals Inc and sold with a lot number SD134 and expiration date 10/31/2026.
Look for the NDC code 13709-325-01 on the label to confirm if you have the recalled product.
The recall states it has sub-potent drug content, which means it may be less effective than labeled. There is no mention of serious injury or harm risks.
The recall does not specify a remedy, so you should check the product details and contact Neilmed Pharmaceuticals for guidance.
Check for the NDC code 13709-325-01 on the label. The product was manufactured by Neilmed Pharmaceuticals Inc with lot number SD134 and expires 10/31/2026.
We’ve drafted a message you can send Neilmed to request your refund or repair — edit it as you like.
Subject: Recall D-0569-2024 — Neilmed Neilmed Hello, I own a Neilmed that is covered by recall D-0569-2024 from Neilmed. 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.
