Hatchet Sanitizer
Product Images NDC 77902-101

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hatchet Sanitizer (NDC 77902-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hatchet Brewing Company, 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

Hatchet Sanitizer 2oz Label (Front)

Hatchet Sanitizer hand sanitizer label features bold black text with the brand name 'Hatchet Sanitizer' and a red shield-shaped emblem containing a black double-headed hatchet. The label states the product is a hand sanitizer and non-sterile solution packaged in a 2 fluid ounce (60 ml) size, with NDC 7790-101-02. The labeler is Hatchet Brewing Company, LLC.*

FDA Label Image

2oz Back (Hbc Hanchet Sanitizer (2oz) Back)

Drug Facts panel for Hatchet Sanitizer, an alcohol antiseptic 80% topical solution. The panel lists the active ingredient as Alcohol 80% v/v with antiseptic purpose, usage instructions, warnings including external use only and flammability, usage restrictions, and directions for application and storage. Inactive ingredients include glycerin, hydrogen peroxide, and purified water. Contact information for Hatchet Brewing Company, LLC of Southern Pines, NC, is provided.*

FDA Label Image

Hatchet Sanitizer 4oz Label (Front)

Hatchet Sanitizer packaging label featuring the product name in large bold black text alongside a red shield emblem with a black hatchet design. The label indicates it is a hand sanitizer non-sterile solution, packaged in a 4 fl oz (120 ml) bottle by Hatchet Brewing Company, LLC. The product NDC is 7790-101-04.*

FDA Label Image

4oz Back (Hbc Hanchet Sanitizer (4oz) Back)

Drug Facts panel for Hatchet Sanitizer showing active ingredient as Alcohol 80% v/v with antiseptic purpose. Includes warnings for external use, flammability, and usage precautions such as avoiding use in children under 2 months and on open wounds. Directions cover application instructions and storage conditions. Inactive ingredients listed as glycerin, hydrogen peroxide, and purified water. Distributed by Hatchet Brewing Company, LLC.*

FDA Label Image

Hatchet Sanitizer 1l Label (Front)

Hatchet Sanitizer packaging label shows the product name in bold black letters alongside a red and black emblem featuring a stylized hatchet. Below, the label specifies it as a hand sanitizer non-sterile solution with a volume of 33.8 fluid ounces (1 liter). The label includes an NDC number 7790-101-33.*

FDA Label Image

1l Back (Hbc Hanchet Sanitizer (1l) Back)

Drug Facts label for Hatchet Sanitizer with 80% alcohol antiseptic topical solution. It includes active ingredient concentration, uses, warnings, directions for use and storage, and inactive ingredients. Distributed by Hatchet Brewing Company, LLC in Southern Pines, NC.*

FDA Label Image

32oz Front (Hbc Hanchet Sanitizer (32oz) Front)

Hatchet Sanitizer packaging label featuring the product name in bold black letters alongside a red arrowhead-shaped logo with a black hatchet symbol. The label states the product as hand sanitizer in a non-sterile solution form with a net volume of 32 fluid ounces (946 ml). The product is labeled by Hatchet Brewing Company, LLC with NDC 7790-101-32.*

FDA Label Image

32oz Back (Hbc Hanchet Sanitizer (32oz) Back)

Drug Facts panel for Hatchet Sanitizer Alcohol Antiseptic 80% Topical Solution distributed by Hatchet Brewing Company, LLC. The label lists alcohol 80% v/v as the active ingredient with antiseptic purpose. It includes uses, warnings for external use and flammability, do not use guidelines, directions for use and storage, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water.*

* 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.