Blackfork Spirits, Llc Hand Sanitizer
Product Images NDC 75093-001

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Blackfork Spirits, Llc Hand Sanitizer (NDC 75093-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blackfork Spirits, 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

Us (Drug Facts)

Drug Facts panel for BlackFork Spirits, LLC Hand Sanitizer showing active ingredient Alcohol 80% v/v as an antiseptic. Includes warnings, directions for use, storage conditions, inactive ingredients (glycerol, hydrogen peroxide, purified water), and manufacturer information. The panel also references temporary policy compliance for alcohol-based hand sanitizers during the COVID-19 emergency.*

FDA Label Image

Front (Front Label 16oz)

Label for Clean-Job Hand Sanitizer, professional grade non-sterile topical solution with 80% alcohol. The label indicates a 16 oz quantity. The label does not display the BlackFork Spirits, LLC name or NDC.*

FDA Label Image

Front (Front Label 32oz)

The image shows the label of Clean-Job Hand Sanitizer, a professional grade, non-sterile topical solution containing 80% alcohol. The label indicates a 32-ounce container. The product is marketed under the BlackFork Spirits, LLC label.*

FDA Label Image

Front (Front Label 5 Gal)

Packaging label for Clean-Job Hand Sanitizer, labeled as professional grade non-sterile topical solution containing 80% alcohol. The package size indicated is 5 U.S. gallons. The label does not show the manufacturer, but product data confirms BlackFork Spirits, LLC as labeler.*

* 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.