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Obagi Nu-Derm® System

Transform your skin with the #1 physician-dispensed skin care system that helps correct hyperpigmentation and improve visible signs of skin aging.
Exclusive information and resources available for new Nu-Derm users and experienced users looking to maintain or continue their transformation.

Transform the look of your skin with a clinically proven hyperpigmentation system that corrects unwanted age spots and significantly lightens the look of your skin.1,†

The safety and effectiveness of the system has not been evaluated beyond 24 weeks. If there is no improvement after 12 weeks, please discontinue use of the system. See below for Important Safety Information.

Obagi Nu-Derm System with 1.0% Retinol* Before & After

BEFORE

WEEK 24

Photos have not been retouched. Results may vary.


Obagi Nu-Derm System with 1.0% Retinol* Before & After

BEFORE

WEEK 24

Photos have not been retouched. Results may vary.


Obagi Nu-Derm System with 1.0% Retinol* Before & After

BEFORE

WEEK 24

Photos have not been retouched. Results may vary.


Obagi Nu-Derm System with 1.0% Retinol* Before & After

BEFORE

WEEK 24

Photos have not been retouched. Results may vary.


Obagi Nu-Derm System with 1.0% Retinol* Before & After

BEFORE

WEEK 24

Photos have not been retouched. Results may vary.


*Retinol 1.0% sold separately.

Study results for a 24-week evaluation of the efficacy and tolerability of twice-daily use of the Obagi Nu-Derm Normal to Oily System with 1.0% retinol, N=33

Reference: 1.Obagi Cosmeceuticals LLC. Data on file.

 


Important Safety Information for Obagi Nu-Derm Clear, Blender® and Sunfader

(contains 4% hydroquinone)

CONTRAINDICATIONS:
People with prior history of sensitivity or allergic reaction to this product or any of its ingredients should not use it. The safety of topical hydroquinone use during pregnancy or in children (12 years and under) has not been established.

WARNINGS:
Avoid contact with eyes, nose, mouth, or lips. In case of accidental contact, patient should rinse eyes, nose, mouth, or lips with water and contact physician.

Sunscreen use is an essential aspect of hydroquinone therapy because even minimal sunlight exposure sustains melanocytic activity.

Contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.

PRECAUTIONS (ALSO SEE WARNINGS):
Treatment should be limited to relatively small areas of the body at one time since some patients experience a transient skin reddening and a mild burning sensation, which does not preclude treatment.

Pregnancy Category C: Animal reproduction studies have not been conducted with topical hydroquinone. It is also not known whether hydroquinone can cause fetal harm when used topically on a pregnant woman or affect reproductive capacity. It is not known to what degree, if any, topical hydroquinone is absorbed systemically. Topical hydroquinone should be used on pregnant women only when clearly indicated.

Nursing Mothers: It is not known whether topical hydroquinone is absorbed or excreted in human milk. Caution is advised when topical hydroquinone is used by a nursing mother.

Pediatric Usage: Safety and effectiveness in children below the age of 12 years have not been established.

Use of the product should be discontinued if hypersensitivity to any of the ingredients is noted.