Saniultra Hand Sanitizer
Product Images NDC 76572-101

1 FDA label image from Relief Films, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Saniultra Hand Sanitizer (NDC 76572-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Relief Films, 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.

FDA Label Image

Saniultra Line Art 4-20-20 Revised (Saniultra Line Art 4 20 20 Revised)

Saniultra Line Art 4-20-20 Revised (Saniultra Line Art 4 20 20 Revised)
SANIULTRA Hand Sanitizer packaging label featuring the brand name with hand graphics. The label highlights 70% alcohol content, a 6.5 FL. OZ (192 ML) bottle size, and FDA registered formula. It includes drug facts with active ingredient Ethyl Alcohol 70%, purpose as antiseptic, warnings, directions, other information, and inactive ingredients. The label states it kills 99.9% of bacteria and viruses and is manufactured by Relief Services, Inc. in Los Angeles, CA.*

* 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.