Meli Hands Hand Sanitizer
Product Images NDC 79426-102

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 Meli Hands Hand Sanitizer (NDC 79426-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meli Hands, Llc, 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

7942610202

7942610202
Drug Facts panel for MELI HANDS hand sanitizer with 70% Ethyl Alcohol as the active ingredient. The panel includes purpose, use, warnings, directions, inactive ingredients, and contact information. The front label shows the product name, scent (Citrus Grove), aloe vera and essential oils, volume (2 fl oz / 59 mL), and labeler MELI HANDS, LLC, Dallas, TX.*
FDA Label Image

7942610216

7942610216
Drug Facts panel for MELI HANDS HAND SANITIZER Citrus Grove scent, showing active ingredient Ethyl Alcohol 70% as antiseptic. The panel includes uses, warnings about flammability and external use, directions for application, a list of inactive ingredients such as aloe vera and essential oils, and contact information for questions or comments. The product size is 16 fl. oz. (473 mL), made by MELI HANDS, LLC, Dallas, TX.*
FDA Label Image

7942610232

7942610232
Label for MELI HANDS Hand Sanitizer featuring aloe vera and essential oils in Citrus Grove scent. The label shows the product volume as 32 fl. oz. (946 ml) and includes a Drug Facts panel with ethyl alcohol 70% as the active ingredient. The labeler is MELI HANDS, LLC, Dallas, TX, with website www.melihands.com.*

* 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.