Liberdol Topical Analgesic Spray
Product Images NDC 71262-008

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Liberdol Topical Analgesic (NDC 71262-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viaderma Distribution, 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

Inner Package (Inner Package)

Label for Liberdol Topical Analgesic Spray by ViaDerma Pharma with active ingredients 30% Methyl Salicylate, 10% Menthol, and 4% Camphor. The label shows it is an analgesic spray, in a 1.85 fluid ounce (55 ml) bottle, made in the USA, and includes contact details for ViaDerma Distribution in Las Vegas, NV.*

FDA Label Image

Outer Package (Outer Package)

Liberdol Topical Analgesic Analgesic Spray by ViaDerma Distribution, Inc. Features a white spray bottle with a clear cap on a blue and white box. Active ingredients listed are 30% Methyl Salicylate, 10% Menthol, and 4% Camphor. The label highlights patented transdermal technology and ultra clear formula. Net contents are 1.85 FL OZ (55 ml). Drug facts and warnings are detailed on one panel along with directions and inactive 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.