Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

NDC 0363-6171-09 Walgreens Sinus Pressure Recalled by LNK International, Inc. Due to Mislabeling

Date: October 11, 2022
Company: LNK International, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact LNK International, Inc. directly.

Affected Products

NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough ACETAMINOPHEN/ PAIN RELIEVER DEXTROMETHORPHAN HBr/ COUGH SUPPRESSANT GUAIFENESIN/ EXPECTORANT PHENYLEPHRINE HCl/ NASAL DECONGESTANT Maximum Strength Decongestant Free DISTRIBUTED BY: WALGREENS CO. 200 WILMOT RD., DEERFIELD, IL 60015 walgreens.com

Quantity: 66,384 boxes of twenty tablets each

Why Was This Recalled?

Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About LNK International, Inc.

LNK International, Inc. has 6 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report