FDAOctober 15, 2024drug

OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., Fairfield, NJ 07004, NDC 71399-0039-06.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

CGMP Deviations

What to do

FDA enforcement status: Ongoing

Brands named

akron pharmaakron

UPCs

71399003906

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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