American Red Cross 70% Ethyl Alcohol Hand Sanitizer Gel
Product Images NDC 75742-032

View Photos of 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 American Red Cross 70% Ethyl Alcohol Hand Sanitizer (NDC 75742-032). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Guoyao Jingyue Aerosol Co., Ltd, 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

Label 1 (Label 1)

Label 1 (Label 1)
Label for AMERICAN RED CROSS 70% ETHYL ALCOHOL HAND SANITIZER gel. The label highlights 70% ethyl alcohol as the active ingredient. It includes moisturizing aloe vera and vitamin E, with a net volume of 8 fluid ounces (236 mL). The design features the American Red Cross logo and a pattern of red crosses with the tagline 'ALWAYS READY.'*
FDA Label Image

Label 2 (Label 2)

Label 2 (Label 2)
Label of AMERICAN RED CROSS 70% ETHYL ALCOHOL HAND SANITIZER topical gel containing 70% ethyl alcohol. The label features blue text and design elements on a white background, highlighting moisturizing ingredients Aloe Vera and Vitamin E. The bottle size is 8 FL OZ (236 mL).*
FDA Label Image

Label 3 (Label 3)

Label 3 (Label 3)
Drug Facts panel for AMERICAN RED CROSS 70% ETHYL ALCOHOL HAND SANITIZER (ethyl alcohol 70% v/v) topical gel. Includes active ingredient purpose, uses as an antiseptic hand sanitizer, warnings for external use only, avoiding eyes and certain body areas, and first aid instructions. Directions for use, other information about storage, inactive ingredients, and contact information are also present, with a flammability warning and manufacturer details.*

* 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.