Dermarad Relief Emulsion
Product Images NDC 76348-720

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 (NDC 76348-720). 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

750 Kb Dermarad Topical Rehydrating Emulsion 118 mL (3)

750 Kb Dermarad Topical Rehydrating Emulsion 118 mL  (3)
Label for DermaRad Relief Topical Rehydrating Emulsion, containing Allantoin 1% and Lidocaine 4% as active ingredients. The label highlights its use as a topical analgesic and skin protectant. Container size is 4 fluid ounces (118 mL). Labeler is RENU LABORATORIES, LLC, with contact information for DermaMedics LLC, Oklahoma City, OK.*
FDA Label Image

Sealendbox 01.06.2023 Dermarad Lotion Box Reduced File Size Opt Page1 (2)

Sealendbox 01.06.2023 Dermarad Lotion  Box Reduced File Size Opt Page1 (2)
Packaging label for DermaRad Relief Lidocaine Emulsion 4% topical rehydrating emulsion in a 4 fl oz (118 ml) size by RENU LABORATORIES, LLC. The label highlights maximum strength 4% lidocaine and 1% allantoin to protect minor burns and relieve pain and itching. It lists product benefits including skin protection, moisturizing oils, humectants, antioxidants, and suitability for radiation patients. The label also includes drug facts, active ingredients, warnings, and usage directions.*

* 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.