Pain Release Oil
Product Images NDC 70983-006

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pain Release (NDC 70983-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Saje Natural Business 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

Pain Release Deb 10 mL

Pain Release Deb 10 mL
This is a medication used for temporary relief of minor aches and pains in muscles and joints associated with sprains, strains, bruises, and simple backache. It contains Menthol as an active ingredient and is classified as a topical analgesic. It comes with a warning label which cautions against using the product on damaged skin or wounds, bandaging tightly, and contact with the eyes. The medication should also be kept away from children and those with high blood pressure. It should not be used by pregnant or breastfeeding women. The medication can be applied to the affected area up to three to four times daily, and should not be used in children younger than two years of age. Not all of the inactive ingredients are clear due to the text quality.*
FDA Label Image

Pain Release Deb 30 mL

Pain Release Deb 30 mL
This is a warning label and package information for a topical analgesic oil blend produced by Saje Natural Wellness based in Vancouver, Canada. The label indicates that the product should not be used if the security seal is broken or missing. Additionally, the package advises consumers to read all product information before using the product and to keep the package for future reference. The product comes in a 30 ml container and is SKU 10301.*
FDA Label Image

Pain Release Deb 6ml

Pain Release Deb 6ml
This is a description of an over-the-counter drug called "Pain Release". The active ingredient in Pain Release is identified as "Nt 198 Topca ardiesi" and its purpose is for the temporary relief of headaches, muscle aches, and joint pain, including those associated with simple backache and sprains. The product comes with several warnings, including to keep it away from heat or flames, not to use it on open wounds or damaged skin, and to avoid contact with the eyes and mouth. The product is not recommended for children under 2 years of age. The directions suggest applying the product to the affected area no more than 10 times per day. The list of inactive ingredients includes several plant extracts.*

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