Dermarad Relief Post Radiation Calming Liquid
Product Images NDC 76348-970

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 Dermarad Relief Post Radiation Calming (NDC 76348-970). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Renu Laboratories, 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

Package Art (8.8.2022 Dermarad Relief Calming Serum With Lidocaine Label 060922hr (2))

Package Art (8.8.2022 Dermarad Relief Calming Serum With Lidocaine Label 060922hr (2))
Drug Facts panel for DermaRad Relief Post Radiation Calming Serum with 3% Lidocaine topical liquid. The panel lists active ingredient lidocaine 3% as an external analgesic, usage for temporary relief of minor pain and itching, warnings for external use and conditions to stop use, directions for applying up to 3 to 4 times daily, and inactive ingredients including oils and antioxidants. Manufacturer and contact information are also included.*
FDA Label Image

Product Box (8.9.22 254 Kb Dermarad Post Radiation Serum Box 061322 Hr Opt Page1 (2))

Product Box (8.9.22 254 Kb Dermarad Post Radiation Serum Box 061322 Hr Opt Page1 (2))
Packaging label for DermaRad Relief Post Radiation Calming Serum with 3% Lidocaine in a 1.7 FL OZ (50 mL) topical liquid form. The label highlights skin relief benefits for burns, sunburn, skin irritations, and cuts, emphasizing a gentle, silicone-based, moisturizing formula free from emulsifiers, harsh chemicals, and parabens. Manufactured for DermaMedics, LLC, Oklahoma City, OK.*

* 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.