Mokeru Antiseptic Hand Sanitizer
Product Images NDC 78156-001

3 FDA label images from Ashford Textiles Llc · 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 Mokeru Antiseptic Hand Sanitizer (NDC 78156-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ashford Textiles 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

Botle (Botle)

Botle (Botle)
Label for Mokeru Antiseptic Hand Sanitizer by Ashford Textiles LLC showing active ingredient Ethyl Alcohol 65%, with Aloe Vera. The label is green with images of aloe leaves and contains drug facts, manufacturing and expiration dates, and bottle volume of 2 fl oz (60 ml).*
FDA Label Image

Botle2 (Botle2)

Botle2 (Botle2)
Drug Facts panel from Mokeru Antiseptic Hand Sanitizer includes warnings such as flammability and not using in the eyes. Instructions advise thorough drying of hands after application. Other sections cover storage in a cool, dry place, list inactive ingredients as water, aloe vera extract, fragrance, and carbomer, and provide a contact number for questions.*
FDA Label Image

Botle3 (Botle3)

Botle3 (Botle3)
Drug Facts label for Mokeru Antiseptic Hand Sanitizer showing active ingredient ethyl alcohol 65% as an antiseptic. The label includes usage instructions for hand washing to decrease bacteria, warnings for external use and flammability, directions to wet hands and allow to dry, storage information, and a customer service phone number. The label also displays contact information for Ashford Textiles LLC and a recycling symbol.*

* 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.