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

Is NDC 0486-1111-01 recalled?

K Phos Original · 100 TABLET, SOLUBLE in 1 BOTTLE (0486-1111-01)

Yes — this exact package was recalled

2 FDA recalls name the code 0486-1111-01 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
Potassium Phosphate, Monobasic
Strength
POTASSIUM PHOSPHATE, MONOBASIC 500 mg/1
Form
Tablet, Soluble · Oral
Labeler
Beach Products, Inc.
Type
Human Prescription Drug
Product code
0486-1111

Recalls naming this package

Class II · Moderate risk

Potassium Acid Phosphate

Labeling: Label Mixup: POTASSIUM ACID PHOSPHATE, Tablet, 500 mg may have potentially been mislabeled as the following drug: predniSONE, Tablet, 20 mg, NDC 00591544301, Pedigree: AD56879_5, EXP: 5/21/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-917-2014
Class II · Moderate risk

Potassium Acid Phosphate

Labeling: Label Mixup: POTASSIUM ACID PHOSPHATE, Tablet, 500 mg may have potentially been mislabeled as the following drug: predniSONE, Tablet, 20 mg, NDC 00591544301, Pedigree: AD56879_5, EXP: 5/21/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-916-2014

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.