Nano Eye Drop Serum Liquid
Product Images NDC 87762-001

View Photos of 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 Nano Eye Drop Serum (NDC 87762-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Shenzhen Yiyang Zhiting Technology Co., 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

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The packaging label for Laniska Nano Eye Drop Serum features the product name prominently with the tagline 'Deep Repair for Multiple Conditions.' It highlights effective care for dry eye, presbyopia, dry and stinging eyes, and blurred vision. The label lists active ingredient Mentha Piperita Leaf and inactive ingredients including water, sorbitol, 1,2-hexanediol, glycerin, and sodium hyaluronate. The 30 mL sterile liquid dropper bottle is marked with usage instructions, warnings, shelf life of 3 years, and contact information for Googeer Ltd, London. A large close-up eye graphic is also visible.*
FDA Label Image

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2 (Screenshot 2026 06 05 121905 069)
Label for Laniska Nano Eye Drop Serum, a topical liquid eye drop. The label highlights the product's use for eye fatigue, dry eye, presbyopia, and blurred vision. It lists active ingredient Mentha Piperita Leaf and inactive ingredients including water, sorbitol, 1,2-hexanediol, glycerin, and sodium hyaluronate. The bottle volume is 30 mL (1 FL OZ), produced by Googeer Ltd, made in China, with a shelf life of 3 years.*

* 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.