Amcinonide Ointment
Product Images NDC 73308-407

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amcinonide (NDC 73308-407). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ayurax, 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

Package Label – Principal Display Panel – 60 G Carton (Amcinonide Carton Label)

Package Label – Principal Display Panel – 60 G Carton (Amcinonide Carton Label)
Box packaging label for Amcinonide Ointment USP 0.1% by Ayurax, LLC. The 60-gram topical ointment label includes NDC 73308-407-60, usage warnings, storage instructions, and directions for opening and closing the tube. The label lists the active ingredient amcinonide 1 mg per gram and inactive ingredients, emphasizing the product is for dermatologic use only and not for ophthalmic use.*
FDA Label Image

Package Label – Principal Display Panel – 60 G Container (Amcinonide Tube Label)

Package Label – Principal Display Panel – 60 G Container (Amcinonide Tube Label)
Label for Amcinonide ointment USP, 0.1%, topical ointment containing 1 mg/g of amcinonide. Manufactured by Ayurax, LLC and distributed by Solubiomix, LLC. The label states usual dosage, warnings, storage instructions, and net weight of 60 grams. It includes an NDC number 73308-407-60 and a barcode.*
FDA Label Image

Chemical Formula (Chemical Structure)

Chemical Formula (Chemical Structure)
Chemical structure diagram of amcinonide, showing its molecular formula C28H35FO7 and a molecular weight of 502.58.*

* 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.