Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 0536-4306-11 recalled?

Fiber Lax · 90 TABLET, FILM COATED in 1 BOTTLE (0536-4306-11)

Yes — this exact package was recalled

1 FDA recall names the code 0536-4306-11 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
Calcium Polycarbophil
Strength
CALCIUM POLYCARBOPHIL 625 mg/1
Form
Tablet, Film Coated · Oral
Labeler
Rugby Laboratories
Type
Human OTC Drug
Product code
0536-4306

Recalls naming this package

Class II ยท Moderate risk

Calcium Polycarbophil

Labeling: Label Mixup: CALCIUM POLYCARBOPHIL, Tablet, 625 mg may have potentially been mislabeled as the following drug: CAFFEINE, Tablet, 100 mg (1/2 of 200 mg), NDC 24385060173, Pedigree: ADWA00002146, EXP: 5/31/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-939-2014

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