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)

Neutrogena Sun Rescue After Sun Medicated Relief Gel provides pain relief and soothes sunburned skin. Its active ingredient, camphor, acts as an external analgesic that temporarily relieves pain and itching. It also contains inactive ingredients such as water, alcohol denat., triethanolamine, carbomer, and EDTA. The gel is safe for adults and children above 2 years of age, but children below 2 years should ask a doctor before use. The product is flammable, hence should be kept away from fire, and contact with eyes should be avoided. It is distributed by Johnson & Johnson Consumer Inc. and is a dermatologist recommended brand.*

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