Sanivir Hands, Body, And Surfaces Sanitizer
Product Images NDC 77396-001

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Sanivir Hands, Body, And Surfaces Sanitizer (NDC 77396-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kemix Quimica, S.a. De C.v., 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

Sanivir 1000 Lts Final

Label for SANIVIR Gel Plus Hand Sanitizer by Kemix Quimica, S.A. de C.V. The label states usage for hands, body, and surfaces with active ingredients Didecyl Dimethyl Ammonium Chloride and Benzalkonium Chloride. It includes safety warnings, storage instructions, a pollution rate index, NFPA hazard ratings, and directions for use. The product is transparent blue liquid with a net content of 1000 liters (219.97 gallons), made in Mexico.*

FDA Label Image

Sanivir 5 Lts Final

SANIVIR Gel Plus Hand Sanitizer by Kemix Quimica, S.A. de C.V. is a hands, body, and surfaces sanitizer with a neutral pH formula. The label indicates active ingredients didecyl dimethyl ammonium chloride and benzalkonium chloride, volume of 5 liters (1.32 gallons), and usage directions for various surfaces. It includes safety warnings, an NFPA hazard indicator, and eco-friendly logos, noting the product is made in Mexico.*

FDA Label Image

Sanivir 75ml Final

Label for SANIVIR Hand Sanitizer gel by Kemix Quimica, S.A. de C.V. The label features a blue background with the product name prominently displayed. It states the volume as 75 mL (2.5 fl oz) and includes a note claiming it kills 99% of viruses and bacteria. The label also shows a barcode, manufacturing information, and an FDA NDC number 77396-001-03. A red cross symbol is centered near the bottom.*

FDA Label Image

Sanivir Gel Plus 5 Lt Final

Label of SANIVIR Gel Plus Hand Sanitizer by Kemix Quimica, S.A. de C.V. The label details uses, directions, warnings, storage, and active ingredients including Didecyl Dimethyl Ammonium Chloride and Benzalkonium Chloride. It shows a hazard warning for eye irritation, NFPA ratings, pollution rate, and net content of 5 liters (1.32 gallons). Made in Mexico with a transparent blue gel containing alcohol odor.*

FDA Label Image

Sanivir Gel Plus 75ml Final

SANIVIR Gel Plus Hand Sanitizer label from Kemix Quimica, S.A. de C.V. The label shows the product name with 'GelPlus' prominently featured, claims to kill 99% of viruses and bacteria, and indicates a volume of 75 mL (2.5 fl oz). It includes a Drug Facts panel detailing active ingredients didecyl dimethyl ammonium chloride 0.25% and benzalkonium chloride 0.1%, uses, warnings, directions, and inactive ingredients. The label is blue with a medical cross symbol and a barcode on the left.*

FDA Label Image

Sva Abn3c2af4759d4c 003761

A certificate of analysis from Batab Health Care SA de CV for Sanivir Sanitizante Virucida, manufactured by Kemix Química SA de CV. It provides quantitative chemical analysis results of the product's ingredients, including purified water (88.63%), ethyl alcohol (8%), isopropyl alcohol (2%), glycerin (0.5%), didecyl dimethyl ammonium chloride (0.25%), benzalkonium chloride (0.1%), and triethanolamine (0.02%). The document is dated 01/09/2020 and signed by a quality analyst.*

FDA Label Image

Svg Brn3c2af4759d4c 004379

A certificate of analysis from Batab Health Care SA de CV for SANIVIR Gel Plus Hand Sanitizer, dated 29/10/2020. The document lists quantitative chemical analysis results showing concentrations of purified water (29.13%), ethyl alcohol (70%), glycerin (0.5%), polyacrylic acid (0.35%), and triethanolamine (0.02%). The certificate is signed by a laboratory quality analyst.*

* 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.