Hand Sanitizer
Product Images NDC 77248-001

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 77248-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Buffalo Distilling Company Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Hand Sanitizer Label (Bdc Handsanitizer)

Hand Sanitizer Label (Bdc Handsanitizer)
This is a description for a hand sanitizer made by the Distilling Company. It is manufactured in accordance with WHO and FDA standards and contains 80% alcohol as an active ingredient to help reduce bacteria on hands. It is an antiseptic hand rub and non-sterile solution. However, it is only for external use and should be kept away from heat and flame. It is not recommended for children under 2 months of age or on open skin wounds. If rash occurs, stop use and consult a doctor as it may be a serious condition. It is advised to supervise children under 8 years of age when using the product. The hand sanitizer should be stored between 15-30 degrees Celsius and contains glycerin, hydrogen peroxide, and purified water as inactive ingredients.*

* 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.