Medline Gel
Product Images NDC 53329-230

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Medline (NDC 53329-230). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medline Industries, Lp, 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

Bottle_back Label (Hh70g04m Bottle Back Label V3 Rl25khi)

Drug Facts panel for Medline Ethyl Alcohol 70% Gel topical antiseptic. Lists active ingredient as ethyl alcohol 70%, usage to decrease bacteria on skin, warnings about flammability and external use, directions for hand application, and other information including inactive ingredients. Also includes manufacturer, barcode, and contact information.*

FDA Label Image

Bottle_front Label (Hh70g04m Bottle Front Label V3 Rl25khi)

Label for Medline Spectrum Advanced Gel Hand Sanitizer featuring 70% ethyl alcohol as the active ingredient. The label shows the Medline logo at the top, product name "Spectrum Advanced," and indicates the dosage form as gel hand sanitizer. The package size is 4 fluid ounces (118 mL).*

FDA Label Image

Packet Label (Hh70gpacketm Packet Label V3 Rl25khi)

Drug Facts panel for Medline Spectrum Advanced Gel Hand Sanitizer with 70% Ethyl Alcohol as the active ingredient. The panel includes purpose (antiseptic), uses, warnings, directions for use, other information, and a list of inactive ingredients. Additional packaging details and a barcode appear below the panel along with the Medline logo and product quantity of 0.08 FL OZ (2.4 mL).*

* 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.