Allergy Relief D recall: Failed Dissolution
Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release Tablets USP, packaged as (a) 20 count carton NDC 49032-273-20; (b) 30 count carton, NDC49032-273-30; Distributed by: Walmart Inc., Bentonville, AR 72716, Product of India
Why was Allergy Relief D recalled?
Failed dissolution specifications
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# (a) AC2203133B, EXP 01/2024; (b) AC2203133A, EXP 01/2024.
- Product
- Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release Tablets USP, packaged as (a) 20 count carton NDC 49032-273-20; (b) 30 count carton, NDC49032-273-30; Distributed by: Walmart Inc., Bentonville, AR 72716, Product of India
- Recalling firm
- Dr. Reddy's Laboratories, Inc.
- Quantity
- 25,176, 30-count; 22,968 20-count
- Distribution
- Nationwide in the USA
- Recall date
- December 7, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)