Terbinafine Hydrochloride
Product Images NDC 54868-5992

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Terbinafine Hydrochloride (NDC 54868-5992). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, Inc., 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

Principal Display Panel (30 g Carton)

Principal Display Panel (30 g Carton)
Packaging label for Terbinafine Hydrochloride 1% cream, OTC, distributed by Physicians Total Care, Inc. The label includes the product NDC 54868-5992 and shows a lot number and expiration date, along with a barcode.*
FDA Label Image

Figure 1 (Terbinafine 01)

Figure 1 (Terbinafine 01)
Illustration showing five toes with target-like circular marks on the toenails, possibly indicating areas of concern or treatment focus on each nail.*
FDA Label Image

Figure 2 (Terbinafine 02)

Figure 2 (Terbinafine 02)
An anatomical illustration showing the side view of a human foot, highlighting the location of the big toe and the area above the ankle with target markers. This figure appears to indicate specific points on the foot and ankle, likely related to application or treatment sites.*
FDA Label Image

Carton (Terbinafine 03)

Carton (Terbinafine 03)
Packaging label for Terbinafine Hydrochloride Cream 1%, an antifungal cream by Physicians Total Care, Inc. The label highlights it as a full prescription strength product for athlete's foot, with a net weight of 1 oz (30 g). It includes usage directions, warnings, inactive ingredients, and a barcode, with a blue color scheme and a foot illustration.*

* 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.