Solaroguard Hand Sanitizer Liquid Solution 80% Topical Solution
Product Images NDC 74705-928

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Solaroguard Hand Sanitizer Liquid Solution 80% Topical Solution (NDC 74705-928). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solarogen, 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

A6175332 5419 B778 E053 2a95a90a3a5d

SolaroGuard Hand Sanitizer Gel 80% Alcohol Antiseptic Solution in a large translucent plastic bottle with a white cap and a front label showing the Solarogen logo, product name, alcohol concentration, non-sterile solution note, lot number, and NDC code 74705-0340. The background shows a brown cardboard box with a matching label including drug facts and instructions. The labeler is Solarogen, LLC.*

FDA Label Image

A71faa58 F1a2 64cf E053 2a95a90a843d

Packaged container of SolaroGuard Hand Sanitizer Gel 80% topical solution by Solarogen, LLC. The image shows a large white gallon bottle with a screw cap featuring a front label with the product name, strength, and type as an alcohol antiseptic non-sterile hand sanitizer gel. Next to it is a cardboard shipping box with a matching product label.*

FDA Label Image

946.37ml Label (Solaroguard Jpg)

Label for SolaroGuard Hand Sanitizer Gel Rub 80% Topical Solution by Solarogen, LLC. The label states it is an alcohol antiseptic 80% solution, hand sanitizer, and non-sterile solution. The manufacturer address is 301 Brentwood St, High Point, NC 27260.*

FDA Label Image

946.37 mL Label Back (Solaroguardback Jpg)

Drug facts and usage instructions panel for SolaroGuard Hand Sanitizer Gel Rub 80% Topical Solution. Includes directions, warnings about flammability and prohibited use in children under 2 months and on open wounds, storage guidelines, and active ingredients such as glycerin and hydrogen peroxide.*

* 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.