Home / drug / D-0199-2025 Class III Reported 2025-01-22
Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46, Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8026-02. Recalled by Akron Pharma, Inc.
Reason for Recall Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
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Recall Number D-0199-2025
Classification Class III
Status Ongoing
Category drug
Initiated 2024-12-12
Reported 2025-01-22
Distribution Nationwide in the US
Code Info Lot: KDC0224001B Exp 09/30/2026 Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer .