Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 57896-0401-10 recalled?

Stool Softener · 1000 CAPSULE, LIQUID FILLED in 1 BOTTLE (57896-401-10)

Yes — this exact package was recalled

1 FDA recall names the code 57896-0401-10 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Docusate Sodium
Strength
DOCUSATE SODIUM 100 mg/1
Form
Capsule, Liquid Filled · Oral
Labeler
Geri-Care Pharmaceutical Corp
Type
Human OTC Drug
Product code
57896-0401

Recalls naming this package

Class II · Moderate risk

DOCUSATE SODIUM Capsule

Labeling:Label Mixup; DOCUSATE SODIUM Capsule, 100 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD37063_4, EXP: 5/13/2014; tiZANidine HCl, Tablet, 2 mg, NDC 00378072219, Pedigree: W002975, EXP: 6/11/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-634-2014

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler