Purcol Moisturizing Hand Sanitizer
Product Images NDC 75266-685

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Purcol Moisturizing Hand Sanitizer (NDC 75266-685). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Purocol 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

Label (Label)

Purcol Moisturizing Hand Sanitizer packaging label featuring a white background with turquoise and red accents. It displays the product name, claims of moisturizing with aloe vera, and contains 70% ethyl alcohol. The front states net weight as 2 fl oz (60 ml). The back includes Drug Facts with active ingredient ethyl alcohol 70%, usage instructions, warnings, inactive ingredients listing, manufacturer information (Purcol USA, Dallas, TX), and a barcode.*

FDA Label Image

Label2 (Label2)

Drug Facts panel of Purcol Moisturizing Hand Sanitizer with 70% ethyl alcohol as the active ingredient. It includes sections on uses, warnings, directions, other information, and inactive ingredients. The label states antimicrobial purpose, flammability warning, external use only, and storage conditions. The product contains aloe vera, with a net volume of 8.5 FL oz (251.3 ml). The label also includes the NDC 75266-685-61 and manufacturer information, Purocol LLC, Dallas, TX.*

FDA Label Image

Label3 (Label3)

Purcol Moisturizing Hand Sanitizer label with 70% ethyl alcohol as active ingredient. The label highlights moisturizing properties, mentions aloe vera, and states it kills 99% of germs. Net weight is 16 fluid ounces (473.1 ml). Label includes Drug Facts, directions, warnings, inactive ingredients, and manufacturer Purocol LLC, Dallas, TX.*

* 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.