Meni Hand Sanitizer
Product Images NDC 79439-000

3 FDA label images from Seekr Global Inc. · 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 Meni Hand Sanitizer (NDC 79439-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Seekr Global 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.

Product Images & Figures Index

FDA Label Image

Bottle (Bottle)

Bottle (Bottle)
Meni Hand Sanitizer Gel packaging label with 70% alcohol content, volume 4.02 FL OZ (125 ml). The label includes the Seekr Essentials logo and indicates the product is made in Mexico and imported by Seekr Global Inc. Contact and website information are provided. The label also features a Drug Facts panel with active ingredient, uses, warnings, directions, and inactive ingredients.*
FDA Label Image

Bottle2 (Bottle2)

Bottle2 (Bottle2)
Label for Meni Hand Sanitizer Gel containing 70% alcohol in a 16.9 FL OZ (500ml) bottle. The product is labeled by Seekr Global Inc. The label includes drug facts such as active ingredient (ethyl alcohol 70%), uses, warnings, directions, other information, and inactive ingredients. Contact information and barcode are also visible.*
FDA Label Image

Bottle3 (Bottle3)

Bottle3 (Bottle3)
Label for Meni Hand Sanitizer Gel by Seekr Global Inc. It contains 70% alcohol in a 33.8 fluid ounce (1000 ml) bottle. The label includes active ingredient information, usage instructions, warnings, directions, other information, inactive ingredients, and contact details for the manufacturer and importer Seekr Global Inc., Austin, TX.*

* 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.