Selenium Sulfide Shampoo
Product Images NDC 16477-422

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Selenium Sulfide (NDC 16477-422). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Laser Pharmaceuticals, 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

Label (16477 422 Label)

Packaging label for Selenium Sulfide 2.25% Shampoo, 6 fluid oz (180 mL), topical use only, not for ophthalmic use. The label includes ingredient and usage instructions, warnings, storage information, and the Laser Pharmaceuticals, LLC logo. The NDC is 16477-422-06. The label is primarily white with a blue square highlighting the product name and strength.*

FDA Label Image

3 Update

This image shows an informational label panel for Selenium Sulfide 2.25% shampoo from Laser Pharmaceuticals, LLC. It includes sections on adverse reactions, overdose, dosage and administration instructions, storage conditions, and legal disclaimers about substitution and bioequivalency. Directions for use for seborrheic dermatitis, dandruff, and tinea versicolor are detailed, along with packaging information for 6 fluid ounce bottles (NDC 16477-422-06).*

FDA Label Image

2 (Label 2)

This panel presents detailed information for Selenium Sulfide 2.25% Shampoo, including its description, clinical pharmacology, pharmacokinetics, indications, contraindications, warnings, precautions, carcinogenesis data, pregnancy category, nursing considerations, and pediatric use. It outlines the shampoo as a topical liquid antiseborrheic and antifungal preparation used for seborrheic dermatitis and related conditions, including safety notes and usage instructions.*

* 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.