Terbinafine Hydrochloride Cream
Product Images NDC 70000-0338

3 FDA label images from Cardinal Health, 110 Dba Leader · 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 Hydrochloride (NDC 70000-0338). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health, 110 Dba Leader, 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

Image (Leader 01)

Image (Leader 01)
An illustration showing the top view of a big toe and several smaller toes. The image includes markings indicating application points or areas on the toenails, likely related to the topical use instructions for Terbinafine Hydrochloride cream 1 g/100g by Cardinal Health, 110 dba LEADER.*
FDA Label Image

Image (Leader 02)

Image (Leader 02)
An instructional diagram showing a foot with emphasis on the toenails, highlighting an area on the big toenail. The illustration likely relates to the topical application of the medication Terbinafine Hydrochloride cream but does not contain visible text or labels.*
FDA Label Image

Principal Display Panel (15 g Tube Carton)

Principal Display Panel (15 g Tube Carton)
Packaging label for Terbinafine Hydrochloride Cream 1%, a topical antifungal cream by Cardinal Health, 110 dba LEADER. The label highlights the product as full prescription strength athlete's foot cream with a net weight of 0.5 oz (15 g). It includes comparison to Lamisil AT active ingredient and states a 100% money-back guarantee. The label also shows directions, warnings, and inactive ingredients on the back panel.*

* 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.