Hand Sanitizer
Product Images NDC 81437-001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 81437-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Innovacion Licorera 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

Zury1 (11111)

Zury1 (11111)
Text panel showing the composition and labeling details for Hand Sanitizer by Innovacion Licorera SA de CV. It specifies undenatured alcohol with 95% ethanol concentration, intended for use in hand sanitizer production with required denaturing. It includes manufacturer address and contact information, FDA registration numbers, and a manufacture date of April 2020.*
FDA Label Image

Zury Label (Img 3438 2)

Zury Label (Img 3438 2)
Text panel describing undenatured alcohol with 95% ethanol concentration, intended for use only in the production of hand sanitizers and requiring denaturing during production. It specifies the product is non-potable and includes labeling and packaging information by Innovacion Licorera S.A. de C.V., with address and contact email provided, as well as FDA registration numbers and a manufacture date of April 2020.*
FDA Label Image

Zury3 (Zury 3)

Zury3 (Zury 3)
A large translucent industrial container wrapped in plastic and secured within a metal frame is shown inside a transport truck. The container features a red diamond-shaped flammable hazard label marked with the number 1170 and the hazard class 3. No other labeling or product details are visible on the container itself.*

* 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.