Hammer Spring Hand Sanitizer
Product Images NDC 76837-001

2 FDA label images from Hammer Spring Distillers · 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 Hammer Spring Hand Sanitizer (NDC 76837-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hammer Spring Distillers, 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

Active Ingredient Section (Fda Back Label)

Active Ingredient Section (Fda Back Label)
Drug Facts panel for Hammer Spring Hand Sanitizer showing active ingredient at 80% alcohol v/v as an antiseptic. The panel includes uses, warnings, directions, other storage information, and inactive ingredients such as glycerine, hydrogen peroxide, and purified water USP. It advises keeping out of reach of children and provides specific usage cautions and storage temperatures. The product size is 1 gallon (3.785 L) with NDC 76837-0001-1.*
FDA Label Image

Principal Display Panel (Fda Front Label)

Principal Display Panel (Fda Front Label)
Label for Hammer Spring Hand Sanitizer, an 80% alcohol antiseptic topical solution. The label states it is a WHO recommended hand rub formulation #1, for external use only, not safe for consumption, and a non-sterile solution. The net weight is 1 gallon (3.78 liters). The label includes the manufacturer information: Hammer Spring Distillers with address in Salt Lake City, Utah, and indicates the product is made in the USA. A circular logo of Hammer Spring Distillers is also present, along with spaces for batch number and date.*

* 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.