Terbinafine Hcl 5%
Product Images NDC 72934-4175

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 Terbinafine Hcl 5% (NDC 72934-4175). 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

Ad (4175 9 End)

Ad (4175 9 End)
Amber plastic bottle with a black child-resistant cap containing TERBINAFINE HCL 5% topical solution by Sincerus Florida, LLC. The label includes instructions for use, storage conditions, and contact information for the manufacturer located in Pompano Beach, FL. The label also has a QR code and mentions reporting adverse reactions to the FDA.*
FDA Label Image

D (4175 9 Front)

D (4175 9 Front)
A small amber bottle with a black screw cap labeled TERBINAFINE HCL USP 5% SOLUTION 15gm. The label shows the NDC number 72934-4175-9 and the brand name Sincerus Florida. It notes the product is a compounded drug made in the USA, with a section indicating Rx only and a BUD date of 01/01/1970.*
FDA Label Image

Qwe (4175 9 Middle)

Qwe (4175 9 Middle)
TERBINAFINE HCL 5% is shown in an amber bottle with a black ribbed cap. The label includes active and inactive ingredient information, directions for use, and the labeler details for Sincerus Florida, LLC. The label advises topical application and provides storage instructions at controlled room temperature.*

* 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.