Nizoral Psoriasis Shampoo
Product Images NDC 55505-202

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nizoral Psoriasis (NDC 55505-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kramer Laboratories, 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

Back Label (Back Label)

Drug Facts panel for Nizoral Psoriasis 3 g/100mL showing active ingredient salicylic acid 3%. It details uses for psoriasis and seborrheic dermatitis symptoms, warnings for external use only, directions for application, storage info, inactive ingredients, and a contact phone number. Distributed by Kramer Laboratories.*

FDA Label Image

Carton (Carton)

Nizoral Psoriasis Salicylic Acid 3% Shampoo & Conditioner packaging label by Kramer Laboratories. The product is labeled to control redness, flaking, and scaling, relieve itching and scalp irritation, and is free of sulfates, dyes, alcohol, artificial fragrances, preservatives, and parabens. The label mentions key ingredients including tea tree oil, green tea, and vitamins E, B5, and C. The bottle size is 11 fl oz (325 mL).*

FDA Label Image

Front Label (Front Label)

Nizoral Psoriasis 3 g/100 mL shampoo and conditioner label by Kramer Laboratories. The label highlights it as a scalp psoriasis shampoo and conditioner containing 3% salicylic acid with tea tree oil. It emphasizes control of redness, flaking, and scaling, relief of itching and scalp irritation, and fast-acting results starting from first use. The product is sulfate, dye, and alcohol-free, presented in an 11 fl oz (325 mL) container.*

* 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.