Elite Pain Relief
Product Images NDC 69418-004

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 Elite Pain Relief (NDC 69418-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meds Direct Rx, 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.

Product Images & Figures Index

FDA Label Image

Eliteback (Eliteback)

Eliteback (Eliteback)
This is a description of an Eleventh pain relief patch that comes with drug facts and details about its ingredients. The active ingredients are allantoin 200% skin protectant, lidocaine Zoox topical anesthetic, and petrolatum 3000% skin protectant. The patch is indicated for the temporary relief of pain associated with minor cuts, scrapes, and burns. The patch should not be used on deep or punctured wounds, animal bites, or serious burns. The directions are to clean and dry the affected area, remove the mesh from backing, and apply to the affected area for up to 10 hours. The patch should not be used for longer than seven consecutive days and children under 12 should consult a physician prior to use. The product is manufactured for Meds Direct R, Inc.*
FDA Label Image

Elitefront (Elitefront)

Elitefront (Elitefront)
This is a pain relief gel by Elite with NDC code 69418-004-15. Its active ingredients include Allantoin at 2%, Lidocaine at 4%, and Petrolatum.*

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