Fluocinolone Acetonide Cream
Product Images NDC 0713-0709

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Fluocinolone Acetonide (NDC 0713-0709). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosette 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

Carton 15g

Packaging label for Fluocinolone Acetonide Cream, USP 0.025%, 15 g tube, a topical prescription drug by Cosette Pharmaceuticals, Inc. The label includes usage warnings, storage instructions, and a barcode. It specifies the product is for topical use only and not for ophthalmic use.*

FDA Label Image

Carton 60g

Packaging label for Fluocinolone Acetonide Cream USP 0.025% topical, 60 g tube, manufactured by Cosette Pharmaceuticals, Inc. The label includes usage warnings, storage instructions, barcode, and a summary of ingredients and dosage directions. Marked Rx only with NDC 0713-0709-60.*

FDA Label Image

Fa Chemical Structure (Structure)

Chemical structure of fluocinolone acetonide, the active ingredient in the product. The structure shows a complex steroid framework with fluorine atoms and hydroxyl groups, representing the molecular layout of this topical corticosteroid compound.*

FDA Label Image

Tube 15g

Label for Fluocinolone Acetonide Cream USP 0.025% topical cream manufactured by Cosette Pharmaceuticals, Inc. The package contains 15 grams. The label states Rx only and warns it is for topical use only and not for ophthalmic use. The label includes the NDC 0713-0709-15 and a barcode. Directions, formula, storage, and manufacturer address are also visible on the label.*

FDA Label Image

Tube 60g

Label for Fluocinolone Acetonide Cream, USP 0.025% topical cream in a 60 g package. The label shows the active ingredient strength, usage warnings, manufacturer Cosette Pharmaceuticals, Inc., and includes the NDC 0713-0709-60. It notes the product is for topical use only and provides storage instructions and opening directions.*

* 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.