Hand Sanitizer Gel
Product Images NDC 76984-434

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer Gel (NDC 76984-434). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Canadian Distribution Channel, 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

76984-434-01 100 mL (76984 434 01 100ml Us Label Gel)

Label for CDC Brands Hand Sanitizer Gel, Alcohol Antiseptic 70% topical solution, 100 ml (3.38 fl. oz). Includes Drug Facts with active ingredient (Alcohol 70% v/v), warnings, directions, inactive ingredients, and storage information. Manufactured by Canadian Distribution Channel in Selwyn, ON, Canada.*

FDA Label Image

76984-434-02 500 mL (76984 434 02 500ml Us Label Gel)

The label panel for CDC Brands Gel Hand Sanitizer CDC70HSG includes drug facts such as 70% v/v alcohol as the active antiseptic ingredient, uses, warnings for external use, directions for application, storage information, and inactive ingredients (glycerin, carbomer 940, hydrogen peroxide, purified water). The panel shows a 500 ml (16.9 fl. oz) container made by Canadian Distribution Channel, featuring a barcode and simple illustrations on how to apply the product.*

FDA Label Image

76984-434-03 1890 mL (76984 434 03 1890ml Us Label Gel)

Drug Facts panel for CDC Brands Gel Hand Sanitizer CDC70HSG with 70% alcohol antiseptic topical solution. It includes active ingredient, uses, warnings, directions, other information, and inactive ingredients. The label notes product volume as 1.89L and provides manufacturer contact details for Canadian Distribution Channel.*

FDA Label Image

2l Ndc 76984-434-04 (76984 434 04 2000ml Us Label Gel)

Drug Facts for CDC Brands Gel Hand Sanitizer CDC70HSG showing active ingredient alcohol 70% v/v as antiseptic, usage for healthcare personnel hand rub, warnings about flammability and use restrictions, directions for use, storage information, inactive ingredients, and a how to apply graphic. The product is a 2L topical solution hand sanitizer, non-sterile, labeled by Canadian Distribution Channel.*

FDA Label Image

3.79l Ndc 76984-434-05 (76984 434 05 3790ml Us Label Gel)

Label for Hand Sanitizer Gel CDC70HSG by Canadian Distribution Channel, alcohol antiseptic 70%, topical non-sterile solution. The label includes the product size 3.79L (128 fl. oz), barcode, directions, warnings, inactive ingredients, and contact information. It also features a "How to Apply" diagram and states it is made in Canada.*

FDA Label Image

300ml Ndc 76984-434-06 (76984 434 06 300ml Us Label Gel)

Drug Facts label for Hand Sanitizer Gel CDC70HSG 70% Alcohol Antiseptic topical hand sanitizer. It states the active ingredient is 70% alcohol with antiseptic purpose. The label includes warnings for external use only, flammability, and precautions for use around children and open wounds. Directions advise applying enough product to cover hands, rubbing until dry, and supervising children under 6. Storage instructions, inactive ingredients (glycerin, carbomer 940, hydrogen peroxide, purified water), and manufacturer contact details from Canadian Distribution Channel are provided. Illustrations show how to apply the sanitizer.*

FDA Label Image

60ml Ndc 76984-434-07 (76984 434 07 60ml Us Label Gel)

Label for CDC Brands Gel Hand Sanitizer CDC70HSG, an alcohol antiseptic 70% topical solution hand sanitizer. The 60 ml (2.0 fl.oz) non-sterile solution is made in Canada by Canadian Distribution Channel. The label includes drug facts, usage directions, warnings, inactive ingredients, and a 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.