Dermarad Relief Emulsion
Product Images NDC 76348-720

2 FDA label images from Renu Laboratories, Llc · 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.

Product Images & Figures Index

FDA Label Image

Dermarad Box (Reduced Dermarad Topical Rehydrating Emulsion 118 mL 5.7.2025)

Dermarad Box (Reduced Dermarad Topical Rehydrating Emulsion 118 mL 5.7.2025)
DermaRad Relief Topical Rehydrating Emulsion label, a lidocaine emulsion for topical application. The label features the product name and logo, indicates 4 fl oz (118 ml) volume, and lists active ingredients including 1% allantoin and 4% lidocaine. The label includes drug facts, usage warnings, directions, inactive ingredients, and manufacturer information for RENU LABORATORIES, LLC.*
FDA Label Image

2025 Box (Sealendbox 01.06.2023 Dermarad Lotion Box Reduced File Size Opt Page1 (2))

2025 Box (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.