US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 10, 2022 (5 years ago)

Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent drug

What was recalled

Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
0363-164-3
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0388-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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