Ciclopirox Olamine 1% / Salicylic Acid 2%
Product Images NDC 72934-7041

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 1% / Salicylic Acid 2% (NDC 72934-7041). 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

Sd (7041 6 End)

Sd (7041 6 End)
White bottle label showing part of the directions and manufacturer information for CICLOPIROX OLAMINE 1% / SALICYLIC ACID 2% topical solution. Directions include use as directed by a physician, hand washing after application, and storage at controlled room temperature. Labeler is Sincerus Florida, LLC, with contact and reporting information to the FDA.*
FDA Label Image

Sf (7041 6 Front)

Sf (7041 6 Front)
CICLOPIROX OLAMINE 1% / SALICYLIC ACID 2% shampoo in a white bottle with a white cap. The label shows the active ingredients and strengths, the product is identified as a compounded drug manufactured by Sincerus Florida, LLC, weighing 120 gm. The NDC number 72934-7041-6 is printed on the label along with a logo featuring the text 'Sincerus Florida'.*
FDA Label Image

Xc (7041 6 Middle)

Xc (7041 6 Middle)
CICLOPIROX OLAMINE 1% / SALICYLIC ACID 2% shampoo bottle label showing active ingredients Ciclopirox Olamine USP 1% and Salicylic Acid USP 2%. Inactive ingredients include Shampoo Base 96.6% and Zinc Pyrithione 50% Dispersion 0.4%. Label also displays Rx only, lot number 351036ABCDEFG@1, and manufacture and expiration dates 01/01/1970 by Sincerus Florida, LLC.*

* 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.