Fluocinonide Solution
Product Images NDC 51672-1273

3 FDA label images from Sun Pharmaceutical Industries, Inc. · 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 Fluocinonide (NDC 51672-1273). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Chemical Structure (Fluocinonide 01)

Chemical Structure (Fluocinonide 01)
Chemical structure diagram of Fluocinonide, showing molecular connectivity and detailed stereochemistry. The image includes the molecular weight (494.54) and molecular formula (C26H32F2O7).*
FDA Label Image

Principal Display Panel (20 mL Bottle Carton)

Principal Display Panel (20 mL Bottle Carton)
Carton label for Fluocinonide Topical Solution USP 0.05%, 20 mL, manufactured by Sun Pharmaceutical Industries, Inc. The label indicates the product is for topical use only and not for ophthalmic use. It includes storage instructions, a barcode, and the NDC 51672-1273-2. The label also displays the Taro logo, indicating distribution or manufacturing by Taro Pharmaceuticals U.S.A., Inc.*
FDA Label Image

Principal Display Panel (20 mL Bottle Carton)

Principal Display Panel (20 mL Bottle Carton)
Packaging label for Fluocinonide Topical Solution USP 0.05%, 20 mL, by Sun Pharmaceutical Industries, Inc. The label shows the product name, strength, dosage form, and warnings for topical use only and keeping medications out of children's reach. The label includes directions to store at 20°-25°C and avoid excessive heat. Manufacturer information and barcode 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.