Hand Sanitizer
Product Images NDC 74308-001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74308-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chainbridge Distillery, Llc, 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

Back Label 177.4ml (Drug Fact Picture)

Back Label 177.4ml (Drug Fact Picture)
Drug Facts panel for Hand Sanitizer by ChainBridge Distillery, LLC lists the active ingredient as Alcohol 80% v/v, serving as an antiseptic. It details uses for reducing bacteria when soap and water are unavailable, warnings including flammability and avoidance in children under 2 months, directions for use on hands, and storage information. Inactive ingredients include glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

Front Label 3785.4 mL (Hand Sanitizer Label 1gal)

Front Label 3785.4 mL (Hand Sanitizer Label 1gal)
Label of Hand Sanitizer by ChainBridge Distillery showing the product as an alcohol antiseptic 80% topical solution. The label states it is a non-sterile solution in a 1 US gallon (3785.4 mL) container. Includes warnings about flammability and external use only, with a fire hazard symbol and manufacturer information.*
FDA Label Image

Front Label 177.4ml (Hand Sanitizer Label 6oz)

Front Label 177.4ml (Hand Sanitizer Label 6oz)
Label for ChainBridge Distillery Hand Sanitizer, an 80% alcohol antiseptic topical solution. The non-sterile solution is packaged in a 6 oz (177.4 mL) container. The label includes a flammable warning and manufacturer details, ChainBridge Distillery, Oakland Park, FL.*

* 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.