Amcinonide
Product Images NDC 0168-0279

3 FDA label images from E. Fougera & Co. A Division Of Fougera Pharmaceuticals, Llc · 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 0168-0279). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by E. Fougera & Co. A Division Of Fougera Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

Chemical Formula (Amc02 0003 01)

Chemical Formula (Amc02 0003 01)
Chemical structure diagram of Amcinonide, showing the molecular formula C28H35FO7 and a molecular weight of 502.58. The structure includes various functional groups and a cyclopentane ring typical of corticosteroid compounds.*
FDA Label Image

Package Label – Principal Display Panel – 60 G Container (Amc02 0003 02)

Package Label – Principal Display Panel – 60 G Container (Amc02 0003 02)
Amcinonide ointment USP 0.1% label from E. Fougera & Co., a division of Fougera Pharmaceuticals, LLC. The label includes dosage instructions to apply twice daily, a warning to keep out of reach of children, and instructions to use the cap to puncture the seal. It is for dermatologic use only and not for ophthalmic use. The net weight is 60 grams, with detailed inactive ingredients and storage instructions at controlled room temperature.*
FDA Label Image

Package Label – Principal Display Panel – 60 G Carton (Amc02 0003 03)

Package Label – Principal Display Panel – 60 G Carton (Amc02 0003 03)
Packaging label for Amcinonide Ointment USP, 0.1%, by E. Fougera & Co., a division of Fougera Pharmaceuticals. The label states the medication is for dermatologic use only, with a net weight of 60 grams. Instructions for opening and closing the tube are included alongside warnings and inactive ingredients such as White Petrolatum and Benzyl Alcohol NF. The NDC 0168-0279-60 is printed 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.