Fluocinonide Solution
Product Images NDC 70771-1375

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fluocinonide (NDC 70771-1375). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

Fluocinonide Topical Solution Usp, 0.5% (3b9bda1e 7644 42e1 9684 6d5379aff56a 02)

This is a topical solution of Fluocinonide with a strength of 0.05% available in a 20 mL bottle. It is for topical use only and should not be used for ophthalmic purposes. It is a prescription-only medication made by Zydus Hormaceauticals.*

FDA Label Image

Image (3b9bda1e 7644 42e1 9684 6d5379aff56a 03)

This is a medication containing 0.5 mg of Flucinonide, USP as a solution of an organic acid monohydrate, dehydrated alcohol, isopropyl adipate, propylene glycol and purified water. The usual dosage involves applying a small amount to the affected area up to four times a day as needed. The medication should be stored between 20 to 25 degrees Celsius and away from excessive heat. The manufacturing company is Cadis Healthcare Ltd, located in Changodar, Ahmedabad, India. Keep this medication out of reach of children. Further information can be found in the package insert.*

FDA Label Image

Fluocinonide Topical Solution Usp, 0.05% (3b9bda1e 7644 42e1 9684 6d5379aff56a 04)

This is a description of Fluocinonide topical solution USP 0.05%, a medication intended for topical use (on skin) only. The solution comes in a 20 mL bottle and contains Fluocinonide USP, an active component used for treating dermatitis, eczema, psoriasis, and other skin conditions. The solution also contains other inactive ingredients such as propylene glycol, purified water, and dehydrated alcohol. The recommended dose is a small amount applied to the affected area two to four times per day, as needed. The insert label provides all prescribing information, and it is essential to keep this medication out of the reach of children. It should be stored between 20°C to 25°C (68°F to 77°F) and protected from excessive heat above 40°C (108°F). The manufacturer is Cadia Healthcare Ltd, located in Changodar, Ahmedabad, India.*

* 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.