Fluconazole Powder, For Suspension
Product Images NDC 72673-091

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 Fluconazole (NDC 72673-091). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Poly Pharm. Co., Ltd., 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

Package Label-principal Display Panel (40 mg/mL (35 mL Bottle))

Package Label-principal Display Panel (40 mg/mL (35 mL Bottle))
Fluconazole 40 mg/mL oral suspension powder label by Zhejiang Poly Pharm. Co., Ltd. The label states the product is for oral use only and contains 1400 mg fluconazole total in a 35 mL volume when reconstituted, with each 5 mL teaspoon containing 200 mg fluconazole. Storage instructions include storing dry powder at controlled room temperature before reconstitution, and suspension between 30°C and 5°C after reconstitution, discarding unused portion after 2 weeks. The product is Rx only.*
FDA Label Image

Package Label-principal Display Panel (40 mg/mL Carton Label)

Package Label-principal Display Panel (40 mg/mL Carton Label)
Fluconazole 40 mg/mL powder for oral suspension USP label, manufactured by Zhejiang Poly Pharm. Co., Ltd. The label indicates a reconstituted volume of 35 mL and includes instructions for mixing, storage, and usage. It is marked Rx only and features the POLY PHARM logo on a green band.*
FDA Label Image

Chemical Structure (Fluconazole Str)

Chemical Structure (Fluconazole Str)
Chemical structure diagram of Fluconazole, showing its molecular framework including triazole rings, a difluorophenyl group, and a hydroxyl functional group.*

* 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.