Clenziderm Pore Therapy Liquid
Product Images NDC 62032-612

3 FDA label images from Obagi Cosmeceuticals Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Clenziderm Pore Therapy (NDC 62032-612). 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

Principal Display Panel (Kit Carton)

Principal Display Panel (Kit Carton)
Obagi Skintrinsiq Clarifying Protocol Kit packaging label showing a white box with gray accents. The front displays the product name "Clarifying Protocol Kit" and lists included items such as Obagi Nu-Derm Gentle Cleanser, Toner, CLENZIderm Pore Therapy, Hydrate Facial Moisturizer, and Sun Shield Mineral Broad Spectrum SPF 50 Sunscreen. The back side indicates the kit provides 30 treatments with 60 tips, includes usage information instructions, and features the Obagi Cosmeceuticals LLC manufacturer details and barcode.*
FDA Label Image

Principal Display Panel (148 mL Bottle Label)

Principal Display Panel (148 mL Bottle Label)
Obagi Medical Clenziderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment label for a 5 FL. OZ. (148 mL) product. The label highlights salicylic acid 2% as the active ingredient used for acne treatment, with drug facts including uses, warnings, directions, other information, and inactive ingredients. Distributed by Obagi Cosmeceuticals LLC, the label details storage instructions and contact information.*
FDA Label Image

Principal Display Panel (85 g Tube Carton)

Principal Display Panel (85 g Tube Carton)
Label for Obagi Medical Sun Shield Mineral Broad Spectrum SPF 50 sunscreen lotion. The label states the product is non-comedogenic and dermatologist tested, with a net weight of 3 oz (85 g). It contains titanium dioxide and zinc oxide as active ingredients. The label includes detailed drug facts, uses, warnings, directions, and a list of inactive ingredients. The product is distributed by Obagi Cosmeceuticals LLC in Long Beach, CA.*

* 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.