Olux
Product Images NDC 54868-5421

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 Olux (NDC 54868-5421). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Chemical Structure Of Clobetasol Propionate (12b72763 47bf 441c 9328 59b85ed700f5 01)

FDA Label Image

Instructions For Applying Olux Foam (12b72763 47bf 441c 9328 59b85ed700f5 02)

Instructions For Applying Olux Foam (12b72763 47bf 441c 9328 59b85ed700f5 02)
This appears to be instructions for using a product called "OLUX Foam". The instructions are for how to properly dispense the foam and apply it to the skin, as well as safety precautions to take to avoid contact with the eyes or other sensitive areas. The text provides step-by-step guidance for using the product effectively.*
FDA Label Image

Olux 50 G Label (5421)

Olux 50 G Label (5421)
This appears to be the label of a pharmaceutical product called "OLUX" with a 8.05% formula, intended for external use. The label also includes a lot number (0800) and an expiration date of January 2068. The manufacturer or distributor of the product is likely "IC1ANS_TOTAL CARE" and the product is associated with the NDC number 5486854210. The purpose or application of the product is not specified.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.