Nioxin Pro Clinical Scalp Recovery Purifying Shampoo
Product Images NDC 82157-011

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nioxin Pro Clinical Scalp Recovery Purifying (NDC 82157-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wella Operations Us 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

82157-011-20_back (A 99350187955 Back Jpg)

Drug Facts panels for Nioxin PRO CLINICAL SCALP RECOVERY purifying shampoo with pyrithione zinc 1 g/100 mL. The panels include active ingredient information, uses, warnings, directions for use, and a detailed list of inactive ingredients. Manufacturer details and barcode are also visible.*

FDA Label Image

82157-011-20_front (A 99350187955 Front Jpg)

Nioxin PRO CLINICAL SCALP RECOVERY purifying shampoo label featuring the brand and product name prominently. It includes text noting it is for itchy, flaky scalp and that it contains pyrithione zinc. The container size is 200 mL (6.7 FL OZ), and the label shows the product is distributed by Wella Operations US LLC.*

FDA Label Image

82157-011-10_back (A 99350188391 Back Jpg)

The image shows front and back views of a label for Nioxin PRO CLINICAL SCALP RECOVERY purifying shampoo containing 1 g/100 mL of pyrithione zinc. The back label includes a Drug Facts panel detailing the active ingredient, uses, warnings, directions, inactive ingredients, manufacturer information (Wella Operations US LLC), and a barcode.*

FDA Label Image

82157-011-10_front (A 99350188391 Front Jpg)

The image shows the front and back views of a 1-liter bottle of Nioxin PRO CLINICAL SCALP RECOVERY purifying shampoo. The front label highlights its use for anti-dandruff, itchy and flaky scalp, containing pyrithione zinc as the active ingredient. The label notes clinical and dermatological testing. The back of the bottle is not labeled.*

* 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.