“LNK Walgreens Sinus Relief Product Mislabeled as Decongestant-Free.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/34267-lnk-walgreens-sinus-relief-product-mislabeled-as-decongestant-free. Based on FDA recall #D-0014-2023 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0014-2023%22&limit=1).
The FDA announced on Oct. 11, 2022, that LNK International, Inc. is recalling NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough because boxes are mislabeled as "Decongestant Free" despite containing Phenylephrine HCl. According to the FDA, consumers should stop using the product and return it for a refund.
The product boxes are mislabeled to read "Decongestant Free," but the product contains Phenylephrine HCl 5mg. This labeling error poses a risk to consumers who must avoid decongestants.
Context
GovInfoNow's records show LNK International, Inc. has had five other recalls on record since July 18, 2012. Other recent recalls of similar products include Kirkland Severe Cold & Flu Recall (Nov. 14, 2024) and LNK Nighttime Sleep-Aid Tablets Recall (Aug. 4, 2022). Similar recent recalls include Nephron Albuterol Inhaler (March 17, 2026) and Walgreens Saline Nasal Spray with Xylitol Recall (Nov. 12, 2025).
How to tell if you have this one
Check for the product labeled 'Decongestant Free' at Walgreens stores. The NDC code 0363-6171-09 identifies this specific product.
Brand
LNK International
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the label that says 'Decongestant Free' on the product packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #D-0014-2023 (October 11, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0014-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.