Lokara
Product Images NDC 0462-0392

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 Lokara (NDC 0462-0392). 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 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

Structural Formula (Lok00 0002 01)

Structural Formula (Lok00 0002 01)
Chemical structure diagram of a corticosteroid molecule, showing detailed atomic connections and functional groups with clear labeling of carbon, oxygen, and hydrogen atoms and specific bonds.*
FDA Label Image

Package Label – Principal Display Panel – 59ml Container (Lok00 0002 02)

Package Label – Principal Display Panel – 59ml Container (Lok00 0002 02)
LoKara Lotion (desonide lotion 0.05%) 59 mL (2 fl oz) packaging label by E. Fougera & Co. It is indicated for external use only, not for ophthalmic use. The label includes usage instructions, lot number, expiration date, and the product NDC 0462-0392-02.*
FDA Label Image

Package Label – Principal Display Panel – 59ml Carton (Lok00 0002 03)

Package Label – Principal Display Panel – 59ml Carton (Lok00 0002 03)
LoKara Lotion label featuring desonide lotion 0.05% strength in a 59 mL (2 fl oz) carton. The label states it is for external use only, not for ophthalmic use, and is marked Rx only. It includes storage instructions, warnings to keep out of reach of children, and directions to apply a thin film two or three times daily. Manufactured by PharmaDerm, a division of ALTANA Inc., Duluth, GA 30096, USA. The label also contains ingredient information and a barcode.*

* 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.