Hand Sanitizer
Product Images NDC 77524-0010

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 77524-0010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Miracle Origin Hand Sanitizer Gel, 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

1000ml Ndc: 77524-0010-6 (Miracle Origin Hand Sanitizer Cross(1000ml))

Miracle Origin Hand Sanitizer Gel label showing 70% alcohol content. The front label displays the brand name 'Miracle,' the product name, and volume of 1000 ml (33.81 fl. oz). The back label includes detailed Drug Facts covering active ingredient, uses, warnings, directions, inactive ingredients, manufacturer information Korea Miracle People Corporation Co., Ltd, and a barcode. The product is made in Korea.*

FDA Label Image

100ml Ndc:77524-0010-2 (Miracle Origin Hand Sanitizer Cross(100ml))

Drug Facts panel for Miracle Origin Hand Sanitizer Gel, showing active ingredient Alcohol 70% as an antiseptic. The label includes uses for hand sanitizing, warnings for external use only and flammability, caution against use in children under 2 months and open wounds, directions for use, storage instructions, inactive ingredients, and contact information for questions or comments. The label also displays the product name, volume (100ml/3.38 fl.oz), and manufacturer Korea Miracle People Corporation Co.,Ltd.*

FDA Label Image

3780ml Ndc: 77524-0010-7 (Miracle Origin Hand Sanitizer Cross(1gal))

Miracle Origin Hand Sanitizer Gel label showing 70% alcohol antiseptic strength, volume of 1 gallon (127.99 fl. oz). The label includes directions, warnings, uses, inactive ingredients, and contact email for Korea Miracle People Corporation Co., Ltd. Text appears in English with some Korean characters, and a black cross symbol highlights the product name on a red and white background.*

FDA Label Image

300ml Ndc: 77524-0010-3 (Miracle Origin Hand Sanitizer Cross(300ml))

Label for Miracle Origin Hand Sanitizer Gel containing 70% alcohol with a volume of 300ml (10.14 fl. oz). The label displays the brand kmprc MIRACLE and lists Korea Miracle People Corporation Co., Ltd as the manufacturer in South Korea. The Drug Facts panel details active and inactive ingredients, warnings, directions, and contact information.*

FDA Label Image

500ml Ndc: 77524-0010-4 (Miracle Origin Hand Sanitizer Cross(500ml))

Drug Facts panel of Miracle Origin Hand Sanitizer Gel shows active ingredient as 70% alcohol with antiseptic purpose. The panel includes uses for reducing bacteria when soap and water are unavailable, warnings, directions for use, storage information, and inactive ingredients like water and glycerin. Contact email and manufacturer Korea Miracle People Corporation details are also provided.*

FDA Label Image

60ml Ndc: 77524-0010-1 (Miracle Origin Hand Sanitizer Cross(60ml))

Drug Facts panel for Miracle Origin Hand Sanitizer Gel containing 70% alcohol as the active ingredient. The panel lists its antiseptic purpose, usage instructions, warnings, and storage information. It includes directions for proper hand sanitizing and cautions against use in children under 2 months. The inactive ingredients are water, glycerin, triethanolamine, and polyacrylic acid.*

FDA Label Image

700ml Ndc: 77524-0010-5 (Miracle Origin Hand Sanitizer Cross(700ml))

Drug Facts panel for Miracle Origin Hand Sanitizer Gel containing 70% alcohol as the active ingredient. The panel lists uses, warnings, directions, storage instructions, inactive ingredients, and contact information for questions or comments, alongside product branding and packaging details including volume of 700ml (23.66 fl. oz.) and manufacturer Korea Miracle People Corporation Co., Ltd.*

* 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.