Fluorouracil Solution
Product Images NDC 51672-4062

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 Fluorouracil (NDC 51672-4062). 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 (Fluorouracil 01)

Chemical Structure (Fluorouracil 01)
Chemical structure of Fluorouracil, the active ingredient in the topical solution product by Sun Pharmaceutical Industries, Inc. The diagram shows the molecular structure including fluorine, nitrogen, oxygen, and carbon atoms arranged in a pyrimidine ring.*
FDA Label Image

Principal Display Panel (2% w/w Bottle Carton)

Principal Display Panel (2% w/w Bottle Carton)
Carton packaging label for Fluorouracil Topical Solution USP 2% w/w, 10 mL. The label indicates the product is for topical use only and is supplied by Taro Pharmaceuticals. Storage instructions specify 20°C to 25°C. The label includes usage warnings and lists inactive ingredients alongside the active ingredient fluorouracil at 20 mg/mL strength.*
FDA Label Image

Principal Display Panel (5% w/w Bottle Carton)

Principal Display Panel (5% w/w Bottle Carton)
Packaging label for Fluorouracil Topical Solution USP 5% w/w, 10 mL, manufactured by Taro Pharmaceutical Industries Ltd. The label states the generic drug name, strength, dosage form, and usage restrictions, emphasizing topical use only and storage instructions. It includes a barcode, NDC number 51672-4063-1, and warnings to keep out of reach of children.*

* 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.