Ciclopirox 8% / Fluconazole 1% / Terbinafine Hcl 1%
Product Images NDC 72934-4045

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ciclopirox 8% / Fluconazole 1% / Terbinafine Hcl 1% (NDC 72934-4045). 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 (4045 9 End)

The image shows a brown plastic bottle with a black ribbed screw cap. The bottle label includes usage directions and manufacturer contact information for Sincerus Florida, LLC. The label advises applying the product topically as directed by a physician and states it is for external use only. The address given is 3265 W McNab Rd, Pompano Beach, FL 33069, along with phone numbers for reporting adverse reactions.*

FDA Label Image

S (4045 9 Front)

Brown bottle with a white label displaying CICLOPIROX OLAMINE USP 8%, FLUCONAZOLE USP 1%, TERBINAFINE HCL USP 1% solution. The label includes the NDC number 72934-4045-9 and indicates a 15gm quantity. The labeler is Sincerus Florida, LLC, identified by a logo with blue and orange colors on the label. Additional label text includes "Rx only" and batch details.*

FDA Label Image

A (4045 9 Middle)

A brown pharmaceutical bottle with a black ribbed cap and a partially unfolded white label. The label lists active ingredients Ciclopirox Olamine USP 8%, Fluconazole USP 1%, and Terbinafine HCl USP 1%, along with inactive ingredients. Directions for use advise application topically as directed by a physician, for external use only, and to wash hands after use. The label also includes storage instructions and contact information for 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.