Fluocinolone Acetonide
Product Images NDC 10135-670

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Fluocinolone Acetonide (NDC 10135-670). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex Pharmaceuticals 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

Fluocinolone Acetonide Topical Solution Usp, 0.01 % Is Intended For Topical Administration. The Active Component Is The Corticosteroid Fluocinolone Acetonide, Which Has The Chemical Name Pregna- 1, 4-diene-3, 20-dione, 6, 9-difluoro-11, 21-dihydroxy-16, 17-[(1-methylethylidene) Bis (oxy)]-, (6α, 11β, 16α)-. It Has The Following Chemical Structure: (Fluocinolone Acetonide 01)

FDA Label Image

Principal Display Panelndc 10135-0670-61fluocinoloneacetonidetopical Solutionusp, 0.01 %60 mLrx Only (Fluocinolone Acetonide 02)

Principal Display Panelndc 10135-0670-61fluocinoloneacetonidetopical Solutionusp, 0.01 %60 mLrx Only (Fluocinolone Acetonide 02)
This is a medication package containing Fluocinolone Acetonide for external use only. It comes in a water-washable base and should not be used for ophthalmic purposes. It should be kept out of the reach of children. The usual dosage is to apply a small amount to the affected area two to four times a day as needed. The package includes prescribing information and the manufacturer is Marlex Pharmaceuticals based in New Castle, DE. The package was last revised in February 2019. No information about the product's appearance or intended use is provided.*

* 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.