Care Touch Instant Hand Sanitizer
Product Images NDC 70393-005

3 FDA label images from Future Diagnostics 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 Care Touch Instant Hand Sanitizer (NDC 70393-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Future Diagnostics 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

70393 005 28

70393 005 28
Label for Care Touch INSTANT HAND SANITIZER Soothing Gel by Future Diagnostics LLC, packaged in a 1-gallon (3.78L) container. The front highlights its effectiveness against 99.99% of germs. The back lists active ingredient as 75% ethanol and other components, with usage directions, warnings, and manufacturer information including a barcode and customer service phone number.*
FDA Label Image

Crtuch2 (Crtuch005)

Crtuch2 (Crtuch005)
Care Touch INSTANT HAND SANITIZER soothing gel 16.9 fl. oz (500 mL) packaging label. The front displays the brand name, product name, germ-kill claim, and highlights Aloe and Vitamin E. The back features drug facts including the active ingredient ethyl alcohol 75% v/v, directions for use, warnings, ingredient list, manufacturer details (Future Diagnostics LLC), and a barcode.*
FDA Label Image

Crtuch1l

Crtuch1l
Care Touch INSTANT HAND SANITIZER 33.8 fl oz/1L soothing gel label with Aloe and Vitamin E. Front shows product name, claims to kill 99.99% of germs. Back panel lists active ingredient Ethyl Alcohol 75% (v/v), directions for use, warnings, ingredients, manufacturer Future Diagnostics LLC, and barcode.*

* 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.