Cold Sore Treatment
Product Images NDC 50730-2005

2 FDA label images from H And P Industries, Inc. Dba Triad Group · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cold Sore Treatment (NDC 50730-2005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H And P Industries, Inc. Dba Triad Group, 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

Trifold Inner (44 2005c In A0409)

Trifold Inner (44 2005c In A0409)
This image provides directions for use of Cold Sore Treatment by H and P Industries, Inc. It details a three-step application process: 1) Clean the affected area with a washcloth and warm water prior to treatment, 2) Break the vial by removing the paper cap and pinching it to expose the applicator tip, and 3) Rub the medication onto the sore and surrounding area carefully without causing skin damage. Additional safety tips include washing hands after touching a cold sore and keeping the vial out of children’s reach.*
FDA Label Image

Trifold Outer (44 2005c Out A0409)

Trifold Outer (44 2005c Out A0409)
Cold Sore Treatment single application topical antiseptic by H and P Industries, Inc., labeled for treating 1 cold sore or fever blister. The packaging highlights a unique patented applicator that eliminates the need to touch the sore with fingers. The label includes directions, warnings, active ingredient benzalkonium chloride 0.13%, and states the package contains 1 vial of 0.6 mL. Distributed by CVS Pharmacy with quality assurance logos and comparison to Viroxyn.*

* 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.