Golfersskin Sunscreen Zinc
Product Images NDC 75916-0635

2 FDA label images from Skin Alive, Ltd. · 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 Golfersskin Sunscreen Zinc (NDC 75916-0635). 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

Golfersskin Sunscreen Zinc (Golferszinc)

Golfersskin Sunscreen Zinc (Golferszinc)
GolfersSkin Sunscreen Zinc SPF 30+ tube packaging by Skin Alive, Ltd., showing front and back views. The front displays the product name 'GolfersSkin sunscreen zinc' with net weight of 0.30 oz (8.5 g). The back highlights SPF 30+ protection, claims of water and sweat resistance, broad spectrum UVA/UVB protection, and usage instructions to apply liberally to face, nose, and lips.*
FDA Label Image

Golferskin Sunscreen Zinc2 (Golferszinc Outer)

Golferskin Sunscreen Zinc2 (Golferszinc Outer)
GolfersSkin Sunscreen Zinc SPF 30+ label displays the product name prominently along with the SPF rating and key features such as water resistance, broad-spectrum UVA/UVB protection. The label includes active ingredients listings of Octinoxate 7.5%, Titanium Dioxide 2.35%, and Zinc Oxide 4.2%. Directions for use and warnings are provided, emphasizing external use only and avoidance of eye contact. The net weight is 0.30 oz (8.5 g). The label also includes the Skin Alive, Ltd. brand, a barcode, and contact info for adverse event reporting, with origin details stating 'Made in NZ' and a website www.golfersskin.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.