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Class III · Lower riskRecall completed

Allergy Relief D

Unlikely to cause harm — often a labeling or packaging issue.

Does this affect you?
Check your lot numberLot# (a) AC2203133B, EXP 01/2024; (b) AC2203133A, EXP 01/2024.
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Failed dissolution specifications

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Distributed by / forWalmart Inc., Bentonville, AR 72716, Product of India
NDC49032-273-20
Show the full FDA record
Full product labelAllergy 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 firmDr. Reddy's Laboratories, Inc.
DistributionNationwide in the USA
Quantity25,176, 30-count; 22,968 20-count
Recall initiated2022-11-21
Report date2022-12-07
Recall completed2024-08-28
Recall numberD-0073-2023
ClassificationClass III
FDA statusTerminated
Origin on filePrinceton NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.