Ultra Guard
Product Images NDC 77085-100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ultra Guard (NDC 77085-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Midwest Extraction Services 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

A5699181 14ad E1f4 E053 2a95a90a48f4

Drug Facts panel for Ultra Guard Alcohol Antiseptic 80% Topical Solution. It lists the active ingredient as Alcohol 80% v/v with antiseptic purpose. The panel includes uses, warnings about flammability and safety, directions for use, storage instructions, and inactive ingredients such as glycerin and hydrogen peroxide. The packaging size is noted as 1 gallon. Manufactured exclusively for Ultra Guard, Waseca, MN.*

FDA Label Image

3785 mL Label (Ultra Guard Label 1 Gallon)

Ultra Guard Premium Hand Sanitizer alcohol antiseptic 80% topical solution label. The label includes drug facts indicating alcohol 80% as the active ingredient with an antiseptic purpose. It provides warnings, directions, storage information, inactive ingredients, and manufacturer contact details. The product volume is 1 gallon and it is manufactured by Midwest extraction services llc.*

FDA Label Image

Ultra Guard 16oz (Ultra Guard Label 16ozs)

Ultra Guard premium hand sanitizer non-sterile solution with 80% alcohol antiseptic topical solution, packaged in a 16 oz container. The label shows the product name, active ingredient (Alcohol 80%), and manufacturer details including Midwest extraction services llc. Also visible is a partial Drug Facts panel with usage and safety information.*

* 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.