Perrigo Company PLC recalls No Drip Nasal Spray due to contaminated excipient. Products may pose health risks from impurities in manufacturing.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling No Drip Nasal Spray products because they were made with a contaminated ingredient. This could lead to health risks for users who take the spray.
The nasal spray was manufactured using an excipient (a substance added to the product) that was contaminated. This contamination could cause health issues if the product is used.
People who own or use the recalled nasal spray are affected. Those with sensitive health conditions may be at higher risk.
Check for the product name 'No Drip Nasal Spray', oxymetazoline HCl 0.05%, 1 fl oz (30 mL) per bottle. The NDC code is 36800-388-10 with batch number 1FK1233, expiring 01/31/2023.
Look for the NDC code 36800-388-10 and batch number 1FK1233 on the product label.
The recall states the product was made with a contaminated excipient, so it is not safe to use.
Check for the NDC code 36800-388-10 and batch number 1FK1233 on the product label.
The recall does not specify a remedy, so contact Perrigo for guidance.
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0625-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0625-2022 from Perrigo. 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.
