Fluocinonide Ointment
Product Images NDC 70700-146

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fluocinonide (NDC 70700-146). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xiromed Llc, 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

Fluo-15-gram (Fluo 15gram)

Packaging label for Fluocinonide Ointment USP, 0.05%, manufactured for Xiromed LLC. The label indicates the product is for external use only and not for ophthalmic use, with a net weight of 15 grams. Instructions for puncturing the tube seal and storage conditions are included. The NDC number 70700-146-15 appears alongside a barcode.*

FDA Label Image

Fluo-30-gram (Fluo 30gram)

Packaging label for Fluocinonide Ointment USP 0.05%, a topical ointment by Xiromed LLC. The label states the product is for external use only, not for ophthalmic use, and contains 30 grams. It includes storage instructions, an NDC of 70700-146-16, and directions for puncturing the tube seal.*

FDA Label Image

Fluo-60-gram-carton (Fluo 60gram)

Packaging label for Fluocinonide Ointment USP, 0.05%, topical ointment by Xiromed LLC. The label includes the NDC 70700-146-17 and displays a 60 grams package size. It states the product is for external use only, not for ophthalmic use, and is Rx only. Directions for puncturing the tube seal and storage instructions are also included.*

FDA Label Image

Chemical Structure (Fluocinonide 01)

Chemical structure of fluocinonide, the active ingredient shown as a complex steroidal molecular formula with several functional groups including fluorine atoms and an ester group.*

* 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.