Ls30
Product Images NDC 77093-220

3 FDA label images from Vincit Zee Company · 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 Ls30 (NDC 77093-220). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vincit Zee Company, 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

236.59ml Label (Ls30 01)

236.59ml Label (Ls30 01)
Drug Facts label for LS30 Alcohol Antiseptic 70% Topical Solution by ZEE Company. The label lists active ingredient 70% alcohol, usage as a hand sanitizer, warnings about flammability and use restrictions, directions for applying to hands, and storage instructions. Inactive ingredients noted include glycerin, hydrogen peroxide, water, and ammonio methacrylate copolymer.*
FDA Label Image

473.18ml Label (Ls30 02)

473.18ml Label (Ls30 02)
Label for LS30 Alcohol Antiseptic 70% Topical Solution by ZEE Company, Inc. The label states the product name, antiseptic hand rub non-sterile solution, and volume of 473.18 mL. It includes a Drug Facts panel listing alcohol 70% v/v as the active ingredient, warnings, directions, and inactive ingredients.*
FDA Label Image

3785ml Label (Ls30 03)

3785ml Label (Ls30 03)
The image shows a drug facts label for LS30, an Alcohol Antiseptic 70% topical solution labeled as an antiseptic hand rub and non-sterile solution. It includes a drug facts box listing active ingredient (Alcohol 70%), uses, warnings, directions, other storage information, and inactive ingredients. Manufactured for Zee Company, Inc. with volume 3.79 L.*

* 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.