Drugplain

NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL

Hydroquinone, Homosalate, Octisalate, and Zinc Oxide · KIT · OBAGI COSMECEUTICAL LLC

No Recall History
Plain English

NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL is a kit containing hydroquinone, homosalate, octisalate, and zinc oxide. Manufactured by OBAGI COSMECEUTICAL LLC.

Key Facts

Brand Name
NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL
Generic Name
Hydroquinone, Homosalate, Octisalate, and Zinc Oxide
NDC Code (Product)
62032-532
Manufacturer
OBAGI COSMECEUTICAL LLC
Dosage Form
KIT
Marketing Status
Marketing Start
12/02/2019

Recall History

No Recall History

Frequently Asked Questions

What is NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL used for?

NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL contains Hydroquinone, Homosalate, Octisalate, and Zinc Oxide. It is a kit taken as directed. Consult your doctor for specific uses.

Is NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL a controlled substance?

NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL is not classified as a controlled substance by the DEA.

What is the generic name for NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL?

The generic name for NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL is Hydroquinone, Homosalate, Octisalate, and Zinc Oxide. There are 2 other brand versions of Hydroquinone, Homosalate, Octisalate, and Zinc Oxide.

What is the NDC code for NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL ?

The NDC (National Drug Code) for NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL is 62032-532, listed by OBAGI COSMECEUTICAL LLC.

Product NDC

62032-532

Package NDC

62032-532-07

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)