Ethyl Alcohol
Product Images NDC 67151-738

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 Ethyl Alcohol (NDC 67151-738). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Progressive Products, 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

Box (67151 737 02)

Box (67151 737 02)
The image shows a packaging label strip with repeated segments for Waxie brand container carton labeling. Each segment includes the Waxie logo and text indicating the product is sold by Waxie's Enterprises, LLC, with an address in San Diego, CA, a contact phone number, and website. The label states '12/240 CT CANISTERS' and notes the product is made in China, with orientation instructions marked as 'THIS SIDE UP.' There are no specific details about Ethyl Alcohol on this label.*
FDA Label Image

Pic 1 (Pic 1)

Pic 1 (Pic 1)
Label for hand sanitizing wipes with 70% alcohol base, showing item number 389913. The label includes a 'Do Not Flush' symbol and barcode. Sold by Waxie's Enterprises, LLC, located in San Diego, California. The label states the wipes are made in China.*
FDA Label Image

Pic 2 (Pic 2)

Pic 2 (Pic 2)
Packaging label for Waxie Hand Sanitizing Wipes, 70% Alcohol Based, containing 240 pre-moistened towelettes sized 6x6.75 inches. The label includes drug facts in English and Spanish, active ingredient ethyl alcohol 70%, usage directions, warnings, storage instructions, and manufacturer information for Waxie's Enterprises, LLC. The product is marked as antiseptic and not flushable.*

* 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.