Nu-derm Sunfader Lotion
Product Images NDC 62032-116

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nu-derm Sunfader (NDC 62032-116). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Obagi Cosmeceuticals Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Chemical Structure (Nu Derm 01)

Chemical Structure (Nu Derm 01)
Chemical structure of hydroquinone (C6H6O2), showing a benzene ring with two hydroxyl groups attached at opposite positions.*
FDA Label Image

Principal Display Panel (57 g Bottle Label)

Principal Display Panel (57 g Bottle Label)
Obagi Nu-Derm Clear Skin Bleaching & Corrector Cream lotion, containing Hydroquinone USP 4% (40 mg/g). The label indicates it is for prescription use only, in a 2 oz (57g) container. It includes usage warnings, storage instructions, and distributor information from Obagi Cosmeceuticals LLC.*
FDA Label Image

Principal Display Panel (57 g Bottle Label)

Principal Display Panel (57 g Bottle Label)
Obagi NU-DERM Blender PM Skin Lightener & Blending Cream lotion with Hydroquinone USP, 4% (40 mg/g), Rx only. The label includes warnings about avoiding contact with eyes, nose, mouth, lips, and advises on sunscreen use during hydroquinone therapy. Net weight is 2 oz. (57 g). Distributed by Obagi Cosmeceuticals LLC.*
FDA Label Image

Principal Display Panel (57 g Bottle Label)

Principal Display Panel (57 g Bottle Label)
Label for Obagi NU-DERM Sunfader Skin Lightener Lotion with Sunscreen SPF 15 PABA-Free, containing Hydroquinone USP 4% as the active ingredient. The 2 oz (57 g) topical prescription product is distributed by Obagi Cosmeceuticals LLC. The label includes warnings, usage instructions, and ingredients Octinoxate USP 7.5% and Oxybenzone USP 5.5%, emphasizing external use and storage conditions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.