US Drug Recall Register
Class III · Low risk Terminated Initiated Jun 4, 2015 (11 years ago)

Dr Blue Pain Relieving Gel, (4.6% menthol), For temporary relief of minor aches and pains…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Superpotent Drug: Product may not be uniformly blended resulting in non-uniform distribution of the active ingredient menthol.

What was recalled

Dr Blue Pain Relieving Gel, (4.6% menthol), For temporary relief of minor aches and pains of muscles and joints, a) 2 oz. Tube, NDC 10578-035-05, b) 5 oz. Jar, NDC 10578-035-04, Manufactured by Indiana Botanic Gardens, Hobart, IN 46342

Recalling firm
Indiana Botanic Gardens, Inc
NDC code
10578-035-05
Origin
IN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1149-2015

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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