Hand Sanitizer
Product Images NDC 77231-040

7 FDA label images from Gia Evolution Sa De Cv · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 77231-040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gia Evolution Sa De Cv, 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

3785 mL (Urgentrn 128 Floz Label 01)

3785 mL (Urgentrn 128 Floz Label 01)
Label for Urgent RN Hand Sanitizer Antibacterial Gel containing 72% ethyl alcohol. The label features the Urgent RN logo and indicates the product is manufactured for Urgent Response Network in Mayfield Village, Ohio, and is a product of Mexico. The package size is 1 gallon (3.78 L), with details on active ingredients, warnings, and storage instructions included.*
FDA Label Image

500 mL (Urgentrn 16.9 Floz Label 01)

500 mL (Urgentrn 16.9 Floz Label 01)
Label for Hand Sanitizer Antibacterial Gel with 72% ethyl alcohol, 16.9 fl oz (500 mL) bottle size, labeled by GIA EVOLUTION SA DE CV. The label includes the product name, active ingredient concentration, manufacturer information, barcode, and detailed drug facts including warnings, directions, and inactive ingredients.*
FDA Label Image

29.5 mL (Urgentrn 1 Floz Label 01)

29.5 mL (Urgentrn 1 Floz Label 01)
The image shows the packaging label of Urgent RN Hand Sanitizer Antibacterial Gel with 72% ethyl alcohol. The front face of the carton is 6 cm by 6 cm, featuring the product name, strength, and volume of 1 fl oz (29.5 mL). The label includes a barcode and NDC number 77231-010-01. The back or interior label panel provides Drug Facts including active ingredient, uses, warnings, directions, and inactive ingredients. It states the product is manufactured for Urgent Response Network, Mayfield Village, OH, and is labeled as a product of Mexico.*
FDA Label Image

59 mL (Urgentrn 2 Floz Label 01)

59 mL (Urgentrn 2 Floz Label 01)
Label for Urgent RN Hand Sanitizer Antibacterial Gel featuring 72% ethyl alcohol. The front panel includes the brand logo, an open tab indicator, barcode, and volume of 2 fl oz (59 mL). The label also displays the NDC 77231-010-02 and highlights the 72% alcohol content in a red and blue design. Manufactured for Urgent Response Network, product of Mexico.*
FDA Label Image

946 mL (Urgentrn 32 Floz Label 01)

946 mL (Urgentrn 32 Floz Label 01)
Label for Urgent RN Hand Sanitizer Antibacterial Gel containing 72% ethyl alcohol. The label indicates antiseptic use and includes warnings about flammability and usage restrictions. The product volume is 32 fl oz (946 mL), manufactured by Urgent Response in Mexico. The label includes drug facts, directions, storage info, and a list of inactive ingredients.*
FDA Label Image

190 mL (Urgentrn 6 Floz Label 01)

190 mL (Urgentrn 6 Floz Label 01)
Label for URGENT RN Hand Sanitizer Antibacterial Gel containing 72% ethyl alcohol. The label includes directions, active ingredient information, warnings, and storage instructions. The product volume is 6.4 fl oz (190 mL). Manufactured for Urgent RN, with contact details and barcode visible on the label.*
FDA Label Image

237 mL (Urgentrn 8 Floz Label 01)

237 mL (Urgentrn 8 Floz Label 01)
The image shows a packaging label for Urgent RN Hand Sanitizer Antibacterial Gel with 72% ethyl alcohol. The label indicates the product volume as 8 fl oz (237 mL) and displays the NDC 77231-010-03. It includes drug facts such as active ingredient, use, warnings, directions, and other information. The labeler is GIA EVOLUTION SA DE CV, a product of Mexico.*

* 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.