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

Is NDC 62032-0101-36 recalled?

NU-DERM CLEAR Skin Bleaching and Corrector · 57 g in 1 BOTTLE, PLASTIC (62032-101-36)

Yes — this exact package was recalled

1 FDA recall names the code 62032-0101-36 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
Hydroquinone
Strength
HYDROQUINONE 40 mg/g
Form
Cream · Topical
Labeler
Obagi Cosmeceuticals LLC
Type
Human Prescription Drug
Product code
62032-0101

Recalls naming this package

Class II · Moderate risk

Obagi Nu-Derm Clear

Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled bottles were inadvertently introduced into the Obagi Exfoderm Forte packaging line. Therefore customers which ordered Clear RX actually had contents of Exfoderm forte.

Terminated Labeling / mix-up Obagi Medical Products NDC 62032-101-36 D-0234-2015

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