Ethyl Rubbing Alcohol Liquid
Product Images NDC 0395-0040

2 FDA label images from Humco Holding Group, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ethyl Rubbing Alcohol (NDC 0395-0040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Humco Holding Group, 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.

FDA Label Image

New Label (Ethyl Alcoholl 70 New Label)

New Label (Ethyl Alcoholl 70 New Label)
Drug Facts panel for Ethyl Rubbing Alcohol 70% by volume, a first aid antiseptic. Includes indications for use on minor cuts, scrapes, and burns; warnings about external use only, flammability, and consulting a doctor for certain wounds; directions for application; storage advice; inactive ingredients; and a tamper-evident safety seal warning. The label also shows Humco as the manufacturer and contact information.*
FDA Label Image

Principal Display Panelndc 0395-0040-16rubbing Alcoholethyl Alcohol 70%uspfirst Aid Antiseptic16 Fl Oz (1 Pt) 473 mL (Ethyl Rubbing Alcohol 01)

Principal Display Panelndc 0395-0040-16rubbing Alcoholethyl Alcohol 70%uspfirst Aid Antiseptic16 Fl Oz (1 Pt) 473 mL (Ethyl Rubbing Alcohol 01)
Label for Ethyl Rubbing Alcohol USP 70%, a topical liquid antiseptic containing 700 mg/mL ethyl alcohol. The label shows a 16 fl oz (473 mL) bottle by Humco Holding Group, Inc. It highlights uses for first aid antiseptic, massage, rubbing, and sponge bath. The label includes warnings, directions, inactive ingredient (purified water), and contact info for Humco, TX.*

* 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.