One Touch Hand Sanitizer
Product Images NDC 77301-604

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for One Touch Hand Sanitizer (NDC 77301-604). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by One Touch Medical 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

Label (Onetouch 1000mlusfinal3)

Label for One Touch Hand Sanitizer gel with 70% alcohol, unscented with aloe, in a 34 fl oz (1 L) size. The label features a blue and white background with black text, includes drug facts detailing active ingredient alcohol 70% v/v, and lists the labeler as One Touch Medical Inc, Vancouver, BC, Canada.*

FDA Label Image

Label (Onetouch 19lusfinal3)

Label for One Touch Hand Sanitizer gel with 70% alcohol, containing 5 gallons (19 liters). It is unscented with aloe and marketed by One Touch Medical Inc. The label includes a drug facts panel detailing the antiseptic active ingredient, usage instructions, warnings, and inactive ingredients. The design features a stylized hand icon and a blue and white color scheme.*

FDA Label Image

Onetouch 1gallon V4

Label of One Touch Hand Sanitizer gel with 70% alcohol, unscented with aloe, in a 1 gallon (3.78 L) size. The label displays the brand name One Touch, an illustration of a hand pressing a button, and a blue and white color scheme. It includes drug facts, directions, warnings, and inactive ingredients. Manufactured by One Touch Medical Inc in Vancouver, Canada.*

FDA Label Image

Onetouch 1gallonrefill V4

Label for One Touch Hand Sanitizer gel, unscented with aloe, containing 70% alcohol. The label indicates a 1 gallon (3.78 L) refill container. It features the One Touch Medical Inc logo and lists active and inactive ingredients, drug facts, directions, warnings, and usage information. Manufactured in Vancouver, BC, Canada.*

FDA Label Image

Label (Onetouch 250mlusfinal3)

The label of One Touch Hand Sanitizer gel, 70% alcohol, 8.5 fl oz (250 mL), by One Touch Medical Inc. It is unscented with aloe and marked as advanced. The label includes a Drug Facts panel listing the active ingredient as alcohol 70% v/v with antiseptic purpose and inactive ingredients including aloe barbadensis extract, purified water, aminomethyl propanol, carbomer, and glycerin. Directions and warnings for use are detailed. The manufacturer information and barcode are also visible.*

FDA Label Image

Label (Onetouch 500mlusfinal3)

Label for One Touch Hand Sanitizer gel with 70% alcohol, 16.9 fl oz (500 mL), unscented with aloe, manufactured by One Touch Medical Inc. The design features a blue background with black text, a hand icon, and a Drug Facts panel detailing active ingredient, uses, warnings, directions, and inactive ingredients.*

FDA Label Image

Onetouch 55gallonusfinal3 Jedit

Drug Facts panel of One Touch Hand Sanitizer showing active ingredient as Alcohol 70% v/v with antiseptic purpose. The panel includes uses, warnings, directions, and inactive ingredients such as aloe barbadensis extract and glycerin. The label also highlights that the sanitizer is unscented with aloe and contains 70% alcohol, in a 55 Gallons / 208 L size.*

FDA Label Image

Label (Onetouch 60ml Usfinal3)

One Touch Hand Sanitizer gel 70% alcohol 2 fl oz (60 mL) bottle label by One Touch Medical Inc. The label features a blue and black design with text highlighting it as an advanced, unscented hand sanitizer gel containing aloe. The label also includes drug facts with active ingredient, use instructions, warnings, and inactive ingredients, 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.