Reported Nov 3, 2021 · Terminated

AllerClear D-24 hr, (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10/240mg), 15-count blister…

Sun Pharmaceutical Industries Inc.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: SUN PHARMACEUTICAL INDUSTRIES INC · 2 Independence Way · Princeton, NJ · 08540-6620

Is this the product you have?

    • AllerClear D-24 hr
    • (Loratadine and Pseudoephedrine Sulfate
    • Extended-Release Tablets
    • USP 10/240mg)
    • 15-count blister packs
  • Manufactured by
    • Ohm Laboratories Inc
    • 1385 Livingston Avenue
    • North Brunswick
    • NJ 08902
    • NDC 63981-724-15
Lot codes and dates
    • AC09723
    • Exo
    • Date 11/2022
Amount recalled
46,584 blister packs

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

Failed Moisture Limits

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Aug 31, 2023 · Data as of Sep 19, 5:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.