Cosco Hand Saniitizer 80%
Product Images NDC 52261-0000

3 FDA label images from Cosco International, Inc. · 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 Cosco Hand Saniitizer 80% (NDC 52261-0000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosco International, Inc., 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

120ml Label (120ml Label)

120ml Label (120ml Label)
Drug Facts panel for Cosco Hand Sanitizer 80% topical solution, 120 mL. Lists ethyl alcohol 80% v/v as the active antiseptic ingredient. Includes uses, warnings, directions, storage instructions, inactive ingredients, and distributor information for Cosco International Inc., Marietta, GA.*
FDA Label Image

240ml Label (240ml Label)

240ml Label (240ml Label)
Label for Cosco Hand Sanitizer 80% topical solution in a 240 mL container. The label highlights 80% alcohol antiseptic content and non-sterile solution status. It includes Drug Facts detailing active ingredient ethyl alcohol 80%, its use as a hand sanitizer, warnings, directions, storage information, and inactive ingredients. Distributed by Cosco International, Inc.*
FDA Label Image

60ml Label (60ml Label)

60ml Label (60ml Label)
Drug Facts panel from a Cosco Hand Sanitizer 80% topical solution label. It lists Ethyl Alcohol 80% as the active ingredient, describes the product as an antiseptic hand sanitizer, and includes warnings, directions, inactive ingredients, storage instructions, and distributor contact 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.