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

Is NDC 58368-0002-02 recalled?

Neorelief for Muscle Crampling and Restlessness · 56.7 g in 1 BOTTLE, PUMP (58368-002-02)

Yes — this exact package was recalled

1 FDA recall names the code 58368-0002-02 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
topical gel for muscle cramping and restlessness
Strength
CAUSTICUM 4 [hp_X]/g; JATROPHA CURCAS SEED 8 [hp_X]/g…
Form
Gel · Topical
Labeler
BioLyte Laboratories, LLC
Type
Human OTC Drug
Product code
58368-0002

Recalls naming this package

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.