Husky 505 Antiseptic Cleanser
Product Images NDC 63779-505

3 FDA label images from Canberra Corporation · 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 Husky 505 Antiseptic Cleanser (NDC 63779-505). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Canberra Corporation, 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

Bottle Label (Hus02 0000 01)

Bottle Label (Hus02 0000 01)
Drug Facts panel for HUSKY 505 Antiseptic Cleanser by Canberra Corporation. Lists active ingredient Chloroxylenol 1.0% w/w as an antiseptic hand cleanser. Includes uses to reduce bacteria and prevent cross contamination, warnings, directions for use, other information about OSHA compliance, and inactive ingredients. Adjacent panel describes the product as an antiseptic lotion cleanser with moisturizers, detailing its purpose and net content of one gallon (3.78 liters).*
FDA Label Image

Drum Label (Hus02 0000 02)

Drum Label (Hus02 0000 02)
Label of HUSKY 505 Antiseptic Lotion Cleanser by Canberra Corporation. The label highlights it as an antiseptic cleanser for handwashing with moisturizers. It includes a logo of hands washing and notes net content of 55 U.S. gallons. The label also references compliance with OSHA Bloodborne Pathogen Standard and advises to see the Drug Facts panel for more information.*
FDA Label Image

Bag Label (Hus02 0000 03)

Bag Label (Hus02 0000 03)
The label for HUSKY 505 Antiseptic Lotion Cleanser by Canberra Corporation features a black background with turquoise and white text. It is described as a 27 fl oz (800 mL) antiseptic hand cleanser lotion with moisturizers, aimed at reducing bacteria and assisting OSHA bloodborne pathogen compliance. The label includes usage instructions, warnings, and a list of inactive ingredients. The product NDC is 63779-505.*

* 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.