Hand Sanitizer
Product Images NDC 76224-6314

3 FDA label images from Whish Body Products · 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 Hand Sanitizer (NDC 76224-6314). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Whish Body Products, 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

490 mL Label (Boxout 16oz)

490 mL Label (Boxout 16oz)
Label for BodyMed Hand Sanitizer showing a 16.9 fl oz (0.49 L) bottle. The sanitizer contains 70% ethyl alcohol and is fragrance- and dye-free. The label includes the BodyMed logo, drug facts panel detailing active ingredient and usage, and states the product is made in the USA. Dimensions are approximately 8.25 inches by 4 inches.*
FDA Label Image

975 mL Label (Boxout 33oz)

975 mL Label (Boxout 33oz)
Label for BodyMed Hand Sanitizer containing 70% Ethyl Alcohol. The label indicates a net volume of 33 fluid ounces (0.975 liters), highlights 0% fragrance and dyes, and includes Drug Facts, directions, warnings, and inactive ingredients. Manufactured exclusively for BodyMed in Hudson, OH, USA. Barcode and product code BDMHS320Z are visible.*
FDA Label Image

3790 mL Label (Boxout Gallon)

3790 mL Label (Boxout Gallon)
Label for BodyMed Hand Sanitizer containing 70% Ethyl Alcohol, with a net volume of 128 fluid ounces (3.79 liters). The label features the BodyMed logo, product name, active ingredient concentration, usage instructions, warnings, and storage information, 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.