Cold Sore Treatment
Product Images NDC 50730-1001

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 50730-1001). 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 1001c In A0907)

Trifold Inner (44 1001c In A0907)
Instructional diagram for Cold Sore Treatment by H and P Industries, Inc. dba Triad Group. The image shows a three-step application process: 1) Clean the area by washing with warm water, 2) Break the vial by removing the paper cap and exposing the applicator tip, pressing the vial to release medication, and 3) Rub the medication on the sore and surrounding area using the applicator tip, with guidance to keep the applicator saturated and not to rub too hard. It includes safety and usage notes.*
FDA Label Image

Trifold Outer (44 1001c Out A0907)

Trifold Outer (44 1001c Out A0907)
CareOne Cold Sore Treatment topical antiseptic with 0.13% Benzalkonium Chloride active ingredient. The product is for cold sore and fever blister treatment and offers 1 day, 1 dose healing. The label highlights a patented applicator for direct application without fingers. It comes in a package containing 2 valves of 0.4 mL each, distributed by American Sales Company and labeled by H and P Industries, Inc. dba Triad Group.*

* 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.