Sanitelle Instant Hand Sanitizer Gel
Product Images NDC 80068-001

View Photos of 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 Sanitelle Instant Hand Sanitizer Gel (NDC 80068-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bentus Laboratorii, Ooo, 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

80068-001-25 (Upload Instant Gel Sanitelle Bentus 250ml 700 Pix)

80068-001-25 (Upload Instant Gel Sanitelle Bentus 250ml 700 Pix)
Sanitelle Instant Hand Sanitizer Gel packaging label showing it as an 8.45 Fl.oz (250 ml) antiseptic hand sanitizer gel with 80% ethyl alcohol. The label is fragrance-free and includes Drug Facts on the back detailing active ingredient, usage, warnings, directions, storage, inactive ingredients, manufacturer (BENTUS LABORATORII, Moscow, Russia), and distributor information (Flex Technologies, USA). It also displays recycling symbols and product NDC 80068-001-25.*
FDA Label Image

80068-001-50 (Upload Instant Gel Sanitelle Bentus 50ml)

80068-001-50 (Upload Instant Gel Sanitelle Bentus 50ml)
Sanitelle Instant Hand Sanitizer Gel 1.7 Fl. oz (50 ml) bottle label by BENTUS LABORATORII, OOO. The front label highlights 80% ethyl alcohol as active ingredient and states it is fragrance free antiseptic hand sanitizer gel. The back label lists active ingredient, purpose, usage instructions, warnings, directions, inactive ingredients, manufacturer and distributor details, and product NDC 80068-001-50.*

* 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.