Ciclopirox Olamine 0.77% / Clobetasol Propionate 0.05% / Salicylic Acid 3%.
Product Images NDC 72934-7039

3 FDA label images from Sincerus Florida, 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 Ciclopirox Olamine 0.77% / Clobetasol Propionate 0.05% / Salicylic Acid 3%. (NDC 72934-7039). 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.

Product Images & Figures Index

FDA Label Image

Ss (7039 6 End)

Ss (7039 6 End)
The image shows a white bottle with a label containing directions for use and manufacturer information. The label instructs application as directed by a physician, topical use only, and storage at controlled room temperature. It includes Sincerus Florida, LLC's address in Pompano Beach, FL, and contact information for reporting adverse reactions. The bottle cap is also white.*
FDA Label Image

Ad (7039 6 Front)

Ad (7039 6 Front)
A white plastic bottle labeled as CICLOPIROX OLAMINE USP 1%, CLOBETASOL PROPIONATE USP 0.05%, and SALICYLIC ACID USP 3% shampoo, 120 grams. The label includes the NDC 72934-7039-6 and indicates that it is a compounded drug made by Sincerus Florida, LLC in the USA.*
FDA Label Image

Ww (7039 6 Middle)

Ww (7039 6 Middle)
CICLOPIROX OLAMINE 0.77% / CLOBETASOL PROPIONATE 0.05% / SALICYLIC ACID 3% suspension shampoo in a white bottle. The label includes active and inactive ingredient percentages and lists the labeler as Sincerus Florida, LLC. The product NDC is 72934-7039.*

* 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.