Action Hand Sanitizer
Product Images NDC 67106-7719

2 FDA label images from Sky Systems Co. 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 Action Hand Sanitizer (NDC 67106-7719). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sky Systems Co. 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

Action Hand Sanitizer 1000ml Back (Sanitizer 1000ml Back Box.jpg.jpeg)

Action Hand Sanitizer 1000ml Back (Sanitizer 1000ml Back Box.jpg.jpeg)
The Action Hand Sanitizer packaging label from Sky Systems Co. Inc. features a 1000 ml (33 fl. oz.) volume indication with a blue wave design at the bottom. The label includes a 'Made in USA' emblem, manufacturer information in Ontario, CA, and the website www.skysystemscoinc.com. It also includes drug facts, active ingredient Ethyl Alcohol at 75%, and warnings. The label mentions the product is printed on 100% recycled paper and provides contact information and usage directions.*
FDA Label Image

Action Hand Sanitizer 1000ml Front (Sanitizer 1000ml Front Box.jpg)

Action Hand Sanitizer 1000ml Front (Sanitizer 1000ml Front Box.jpg)
Unfolded packaging label for Action Hand Sanitizer by Sky Systems Co. Inc., featuring the SKy logo with "1000 ml Soap System". The label includes loading instructions with illustrations for dispenser use, a "Made in USA" emblem, and a "Perfect Choice" ribbon graphic. Text advises professional use with protection from freezing and excessive heat. A barcode is also visible at the bottom.*

* 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.