Clobetasol Propionate 0.05% / Niacinamide 4%
Product Images NDC 72934-4059

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Clobetasol Propionate 0.05% / Niacinamide 4% (NDC 72934-4059). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sincerus Florida, 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

S (4059 5 End)

This text provides information for reporting adverse reactions and side effects of drugs to the US Food and Drug Administration (FDA) through their website or phone number. It also states that the information is for office use only and not for resale.*

FDA Label Image

D (4059 5 Middle)

This is a description of a topical solution containing two active ingredients: Clobetasol Propionate USP and Niacinamide USP. The former is a corticosteroid used to treat skin conditions such as eczema and psoriasis, while the latter is a form of vitamin B3 that can improve the appearance of skin and reduce inflammation. The solution also contains Ethyl Alcohol USP and Purified Water USP as inactive ingredients.*

FDA Label Image

Z (4059 5)

This is a topical medication with the NDC code 7293440595. It contains Clobetasol Propionate with a strength of 0.05% and Niacinamide USP at a concentration of 4%. The medication comes in the form of a 60gm solution.*

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