Perrigo recalls No Drip Nasal Decongestant due to contaminated ingredients from a supplier. Products may pose health risks. Consumers should check NDC 21130-801-10 and batch 1BK0964.
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Perrigo is recalling No Drip Nasal Decongestant bottles that were made with contaminated ingredients. This could lead to health risks if the product is used.
The product was manufactured using an excipient (ingredient) that was contaminated. This contamination could cause health issues when the product is used.
People who own or use the recalled No Drip Nasal Decongestant product are affected. Those with allergies or sensitive health conditions may be at higher risk.
Check for NDC code 21130-801-10 and batch number 1BK0964 on the bottle. The product was distributed by Better Living Brands and sold until January 31, 2023.
Look for NDC 21130-801-10 and batch 1BK0964 on the bottle label.
The recall states the product was made with contaminated ingredients, so it is not safe to use.
Check for NDC 21130-801-10 and batch number 1BK0964 on the bottle label.
The recall does not specify a remedy, so contact the manufacturer 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-0622-2022 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0622-2022 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.
