Mucus Relief D recall: Subpotent
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
Why was Mucus Relief D recalled?
Subpotent drug
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: AT2102065A, AT2102065B, Exp 04/2023.
- Product
- 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.
- Quantity
- 18336 cartons
- Distribution
- USA Nationwide
- Recall date
- January 26, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)