Fluocinolone Acetonide
Product Images NDC 10135-670

2 FDA label images from Marlex Pharmaceuticals Inc · Packaging, Regulatory Labels, and Product Appearance

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.

Product Images & Figures Index

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)

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)
Chemical structure diagram of fluocinolone acetonide, showing its molecular arrangement including rings and functional groups such as hydroxyl, ketone, and ester moieties.*
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)
Packaging label for fluocinolone acetonide topical solution USP 0.01%, 60 mL, manufactured and distributed by Marlex Pharmaceuticals, Inc. The label states it is for external use only, not for ophthalmic use, and includes handling and storage instructions. The NDC number 10135-0670-61 is visible on the label.*

* 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.