Neutrogena Sun Rescue After Sun Medicated Relief Gel
Product Images NDC 69968-0721

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Neutrogena Sun Rescue After Sun Medicated Relief (NDC 69968-0721). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kenvue Brands 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

Ntg001 (Ntg001)

Drug Facts panel for Neutrogena Sun Rescue After Sun Medicated Relief Gel with 0.45% camphor as the active ingredient. The label includes uses for temporary relief of sunburn pain and itching, warnings for external use and flammability, directions for application, storage information, inactive ingredients, and contact details for consumer questions. Distributed by Johnson & Johnson Consumer Inc.*

* 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.