Nizoral Shampoo
Product Images NDC 55505-232

View Photos of 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 Nizoral (NDC 55505-232). 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)

Back Label (Back Label)
Drug Facts panel for Nizoral Shampoo with ketoconazole 1% w/w as the active ingredient, indicated as an anti-dandruff shampoo. Includes sections for uses, warnings, directions for adults and children 12 years and over, storage information, inactive ingredients, and contact information for questions or comments. Distributed by Kramer Laboratories.*
FDA Label Image

400 mL Carton (Carton)

400 mL Carton (Carton)
Nizoral Anti-Dandruff Shampoo with Ketoconazole 1% strength in a 14 fl oz (400 mL) topical shampoo format. The label highlights the product's anti-dandruff properties, peppermint complex, and tea tree essence for a refreshing scent. Manufactured by Kramer Laboratories, the label includes drug facts, usage instructions, warnings, and distributor information.*
FDA Label Image

Front Label (Front Label)

Front Label (Front Label)
Nizoral Anti-Dandruff Shampoo label containing Ketoconazole 1% topical formulation. The label highlights peppermint complex and tea tree essence ingredients and indicates the product size as 14 fl oz (400 mL). The label emphasizes control of dandruff fungus and refreshing peppermint scent. Labeler information is not visible on the label image.*

* 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.