Snowskin Sunscreen
Product Images NDC 75916-4018

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Snowskin Sunscreen (NDC 75916-4018). 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

Snowskin Sunscreen2 (Snowskin 125ml)

SnowSkin Sunscreen SPF 30+ in a 4.2 fl oz (125 ml) tube labeled as very water and sweat resistant with broad spectrum UVA/UVB protection. The label features the brand name prominently, mentions Manuka Honey UMF 18, and states it is proven in extreme New Zealand conditions. The product is labeled by Skin Alive, Ltd.*

FDA Label Image

Snowskin Sunscreen (Snowskin 40ml)

Label for SnowSkin Sunscreen SPF 30+ by Skin Alive, Ltd., featuring 1.35 fl oz (40 ml) size. The sunscreen is described as very water and sweat resistant, broad spectrum, and offering UVA/UVB protection. Key active ingredients include Octinoxate 7.5%, Oxybenzone 3.45%, Titanium Dioxide 1%, and Zinc Oxide 1.95%. The product contains Manuka Honey UMF 18 and is made in New Zealand. Directions, warnings, and ingredient information are also provided on the label.*

* 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.