Ketoconazole 2% / Salicylic Acid 2%
Product Images NDC 72934-7133

3 FDA label images from Sincerus Florida, 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 Ketoconazole 2% / Salicylic Acid 2% (NDC 72934-7133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, 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.

Product Images & Figures Index

FDA Label Image

Ss (7133 6 End)

Ss (7133 6 End)
KETOCONAZOLE 2% / SALICYLIC ACID 2% topical solution bottle label from Sincerus Florida, LLC. The label includes usage directions advising application as directed by a physician, washing hands after use, and external use only. Storage instructions specify controlled room temperature (20-25°C). Manufacturer contact information and a QR code are also visible.*
FDA Label Image

Sf (7133 6 Front)

Sf (7133 6 Front)
White plastic bottle of KETOCONAZOLE 2% / SALICYLIC ACID 2% shampoo, 120 grams, labeled as a compounded drug. The label includes the NDC number 72934-7133-6 and the Sincerus Florida logo with teal and orange colors. The product is made in the USA.*
FDA Label Image

Sd (7133 6 Middle)

Sd (7133 6 Middle)
KETOCONAZOLE 2% / SALICYLIC ACID 2% shampoo bottle label showing active and inactive ingredients. The label lists Ketoconazole USP 2% and Salicylic Acid USP 2% as active ingredients. Inactive ingredients include Cocamide DEA 2%, Edetate Disodium USP Dihydrate 1%, Lactic Acid USP 1.6%, purified water USP 10%, Suspendisse shampoo 81%, Trolamine NF 0.1%, and Zinc Pyrithione 50% Dispersion 0.4%. Manufacturer information and lot number are also visible.*

* 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.