Biocef Hand Sanitizer
Product Images NDC 80043-070

2 FDA label images from Abdulalim Alismis-ihlas Kimya Temizlik Maddeleri Imalati · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Biocef Hand Sanitizer (NDC 80043-070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Abdulalim Alismis-ihlas Kimya Temizlik Maddeleri Imalati, 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

Biocef 100ml Gel (Biocef 100ml Gel 1)

Biocef 100ml Gel (Biocef 100ml Gel 1)
Label of Biocef Hand Sanitizer featuring 70% alcohol content, designed for antimicrobial use. The front highlights its ability to kill 99.9% of germs and specifies the volume as 3.4 FL OZ (100 mL). The back includes drug facts such as active ingredient Ethyl Alcohol 70%, usage warnings, directions, inactive ingredients, production and expiration dates, distributor information from Soloway Global LLC Virginia, USA, and indicates it is made in Turkey by ABDULALIM ALISMIS-IHLAS KIMYA TEMIZLIK MADDELERI IMALATI.*
FDA Label Image

Biocef 250ml Gel (Biocef 250ml Gel 2)

Biocef 250ml Gel (Biocef 250ml Gel 2)
Label for Biocef Hand Sanitizer containing 70% alcohol content, with a net volume of 8.4 fluid ounces (250 mL). The label states it kills 99.9% of all germs. The product is distributed by Soloway Global LLC, Virginia, USA, and produced by ABDULALIM ALISMIS-IHLAS KIMYA TEMIZLIK MADDELERI IMALATI in Turkey. The label includes warnings, directions, active and inactive ingredient information, and storage instructions.*

* 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.