Orca Complete Menthol Pain Reliever Liquid
Product Images NDC 82939-000

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 Orca Complete Menthol Pain Reliever (NDC 82939-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Orca Products, Llc, 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

Orca Complete Inner Label (Orca Complete Inner Label)

Orca Complete Inner Label (Orca Complete Inner Label)
This is a liquid pain reliever labeled as "COMPLETE MENTHOL", which is natural and clinically proven. The product is not labeled for retail sale, and should only be used for up to 7 days unless directed by a dentist or a doctor. The product should not be used excessively, and if symptoms persist or worsen after 7 days, medical attention is required. The product should be kept away from children, and if tamperproof seal is not intact at the time of first use, do not use. The product is to be used by adults and children over the age of 12 by applying 10-6 drops onto Orcafoam or a similar resorbable gelatin sponge or galize strip and applied to the area of discomfort in the oral region for at least 1 minute and then spat out. The product should be used up to four times a day as directed by a dentist or doctor. For inquiries, you can contact the manufacturer's customer service from Mon-Fri, 8 AM-3 PM CST.*
FDA Label Image

Orca Complete Outer Label (Orca Complete Outer Label)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.