Gentlecare Hand And Skin Sanitizer Liquid
Product Images NDC 78181-020

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gentlecare Hand And Skin Sanitizer (NDC 78181-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Paragon Solutions Us, 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

020-02 (020 02)

The drug facts and product information panel for GentleCare Solutions Foaming Hand & Skin Sanitizer with Benzalkonium Chloride 0.13%. The label details it as an antibacterial, alcohol-free, fragrance-free liquid sanitizer containing aloe vera. It includes usage directions, warnings, inactive ingredients, a reorder number, and contact information for the manufacturer, Paragon Solutions US, Inc.*

FDA Label Image

020-07 (020 07)

Label for GentleCare Hand and Skin Sanitizer by Paragon Solutions US, Inc., a foaming liquid topical sanitizer. Active ingredient is Benzalkonium Chloride 0.13% (antibacterial). The 7.5 fl oz (221 mL) package highlights features like alcohol-free, sting-free, fragrance-free, and moisturizing with aloe vera. Includes Drug Facts, directions, warnings, inactive ingredients, and contact info.*

FDA Label Image

020-28 (020 28)

Label for GentleCare Solutions Foaming Hand & Skin Sanitizer featuring Benzalkonium Chloride 0.13% antibacterial liquid. The label highlights key features: kills 99.99% of germs, alcohol-free, sting-free, moisturizes, conditions, and fragrance-free. It includes directions, warnings, inactive ingredients, and contact information for Paragon Solutions US, Inc. The container size noted is 1 gallon (128 fl oz), with a Made in the USA mark and barcode.*

* 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.