Fluocinolone Acetonide Topical Solution Usp, 0.01% Solution
Product Images NDC 21922-003

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fluocinolone Acetonide Topical Solution Usp, 0.01% (NDC 21922-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Encube Ethicals, 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 Carton Label

Packaging label for Fluocinolone Acetonide Topical Solution USP, 0.01%, a topical solution indicated for prescription use. The label displays the product name prominently, the strength as 0.01%, and volume of 60 mL. It includes the labeler name Encube Ethicals, Inc., and NDC 21922-003-01. Storage instructions and usage warnings state it is for topical use only and not for ophthalmic use. The design features a blue curved element and includes a barcode.*

FDA Label Image

Fluocinolone Acetonide Tube Label

Packaging label for Fluocinolone Acetonide Topical Solution USP, 0.01%, 60 mL solution for topical use only, not for ophthalmic use. The label features the Encube logo and states the product is Rx only. The back includes formulation details, storage instructions, manufacturer and distributor information, a barcode, and a designated area for batch coding including lot and expiry dates.*

FDA Label Image

Structure.jpg (Structure)

Chemical structure of Fluocinolone Acetonide, the active ingredient in Fluocinolone Acetonide Topical Solution USP, 0.01%. The diagram shows the steroid backbone with associated functional groups including hydroxyl, carbonyl, fluorine substituents, and acetonide moiety.*

* 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.