Alclometasone Dipropionate
Product Images NDC 0168-0263

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 Alclometasone Dipropionate (NDC 0168-0263). 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.

FDA Label Image

Alcldiprocr 03

Alcldiprocr 03
Packaging label for Alclometasone Dipropionate Cream USP 0.05% by E. Fougera & Co. The label shows the product name, strength, dosage form (cream), and that it is for dermatologic use only, not for ophthalmic use. The net weight is 15 grams. The label includes dosage instructions, storage conditions, ingredient list, and tamper-resistant seal information. Barcode and NDC 0168-0263-15 are visible.*
FDA Label Image

Alclodiprocr 02

Alclodiprocr 02
Alclometasone Dipropionate Cream USP, 0.05%, topical cream in a 15 gram tube by E. Fougera & Co., a division of Fougera Pharmaceuticals. The label states it is for dermatologic use only and not for ophthalmic use, listing the active ingredient alclometasone dipropionate 0.5 mg per gram along with inactive ingredients. Directions include applying a thin film two to three times daily, with storage instructions and safety warnings.*
FDA Label Image

Alclometasonediprocr 01

Alclometasonediprocr 01
Chemical structure of Alclometasone Dipropionate shown as a detailed molecular diagram, including labeled functional groups and stereochemistry.*

* 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.