Sani Stix
Product Images NDC 79245-000

3 FDA label images from X Auto 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 Sani Stix (NDC 79245-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by X Auto 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

Label (Label)

Label (Label)
Packaging label for Sani Stix hand sanitizer gel by X Auto Inc. The label shows 'HAND SANITIZER GEL' and highlights an active ingredient concentration of 71.5% v/v Ethyl Alcohol. The label includes warnings, drug facts, and the phrase 'Stay Safe Stay Clean.' The design features blue, green, white, and gray colors with the product name prominently displayed.*
FDA Label Image

Label2 (Label2)

Label2 (Label2)
Sani Stix individual-use hand sanitizer packets contain 71.5% v/v ethyl alcohol with eucalyptus mint scent. The packaging shows 36 sticks, each 3.5 mL, designed for travel-friendly use. Labeler is X Auto Inc. The blue pack highlights various use locations such as auto, home, office, gym, and school.*
FDA Label Image

Label3 (Label3)

Label3 (Label3)
Sani Stix individual-use hand sanitizer packets packaging by X Auto Inc. The label shows a blue background with the product name prominently displayed. It contains 71.5% ethanol alcohol as the active ingredient for antiseptic purposes. The package highlights the product as perfect to take anywhere, with warnings, directions, and additional information included on the back, along with a barcode and manufacturer details.*

* 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.