Whitestone Dome Life Hand Sanitizer
Product Images NDC 76941-101

2 FDA label images from White Stone, 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 Whitestone Dome Life Hand Sanitizer (NDC 76941-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by White Stone, 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.

Product Images & Figures Index

FDA Label Image

100ml (Whitestone Dome Life Hand Sanitizer 100ml Label Draft)

100ml (Whitestone Dome Life Hand Sanitizer 100ml Label Draft)
Whitestone Dome Life Hand Sanitizer Gel packaging shows front and back views. The front features the product name, 'Hand Sanitizer Gel (Ethanol)', branding, and a blue graphic of a hand with a droplet. It states 'Kills 99.9% of Germs' and promotes gentle cleansing and rich moisturizing. The back displays Drug Facts including active ingredient Alcohol 74.18% v/v and usage warnings. Manufacturer JUHWANBIO.CELL CO., LTD. and distributor Kreassive LLC addresses, barcode, and website www.whitestonedome.com are also visible.*
FDA Label Image

500ml (Whitestone Dome Life Hand Sanitizer 500ml Label Draft)

500ml (Whitestone Dome Life Hand Sanitizer 500ml Label Draft)
Drug Facts panel for Whitestone Dome Life Hand Sanitizer gel containing ethanol. Lists 74.18% alcohol as the active ingredient with antiseptic purpose. Includes uses, warnings, directions, storage instructions, inactive ingredients, and manufacturer and distributor information. The label emphasizes gentle cleansing, moisturizing, and antibacterial effects.*

* 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.