Cold Sore Treatment Solution/ Drops
Product Images NDC 51393-5013

View Photos of 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 51393-5013). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Forces Of Nature, 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 (4 ml Bottle Carton)

Principal Display Panel (4 ml Bottle Carton)
Packaging label panel for Cold Sore Treatment Extra Strength solution drops by Forces of Nature. The label highlights its homeopathic formula with active ingredients including echinacea angustifolia, sodium chloride, thuja occidentalis, and calendula officinalis. The product is USDA Organic and Non-GMO Project Verified, comes in a 4 mL (0.14 FL OZ) bottle, and is intended for topical use. The label includes manufacturer information, a barcode, and various certification logos.*
FDA Label Image

Principal Display Panel (11 ml Bottle Carton)

Principal Display Panel (11 ml Bottle Carton)
The carton label for Cold Sore Treatment Extra Strength, a topical solution/drops by Forces of Nature. It contains echinacea angustifolia, sodium chloride, thuja occidentalis, and calendula officinalis. The 11 ml (0.37 fl oz) package highlights fast relief of pain and itching, calms redness, reduces tingling and burning, and helps repair skin. The label features certifications for USDA Organic and Non-GMO Project Verified, cruelty-free status, and states the product is made in the USA with globally sourced ingredients.*

* 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.