Surfers Skin Sunscreen
Product Images NDC 75916-4019

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Surfers Skin Sunscreen (NDC 75916-4019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Skin Alive, Ltd., 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

Surfersskin Sunscreen (Surferssunscreen1)

Surfers Skin Sunscreen SPF 30+ in a 4.2 fl oz (125 ml) container from Skin Alive, Ltd. The label highlights very water/sweat resistant, broad spectrum UVA/UVB protection. It also states the presence of Manuka honey UMF 18 and claims proven effectiveness in extreme New Zealand conditions. The backside includes Drug Facts with active ingredients like Octinoxate and Zinc Oxide, usage directions, warnings, and inactive ingredients.*

FDA Label Image

Surfersskin Sunscreen (Surferssunscreen Outer)

Surfers Skin Sunscreen spf30+ label showing a 1.35 fl oz (40 ml) product by Skin Alive, Ltd. The label highlights very water and sweat resistant, broad spectrum UVA/UVB protection, Manuka honey UMF 18, and PABA-free formulation. It includes active ingredients (Octinoxate 7.5%, Oxybenzone 3.45%, Titanium Dioxide 1%, Zinc Oxide 1.95%), drug facts, usage instructions, warnings, and inactive ingredients. The product is made in New Zealand and features the website surfersskin.co.*

* 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.