During the height of the COVID-19 pandemic, many craft distilleries manufactured ethanol-based hand sanitizer under an Emergency Use license from the FDA. The hand sanitizer manufactured at New Deal was the World Health Organization dry-rub Formulation 1 which contains the following ingredients: ethanol 80%, vegetable glycerin, hydrogen peroxide, purified water. This simple and clean sanitizer contains no synthetic fragrances, no artificial preservatives, and no petroleum-based ingredients. The active ingredient in this hand sanitizer is ethanol, which effectively inactivates a wide array of potentially harmful microorganisms on hands. It is a clear liquid with a watery consistency that dries very fast. You can view our official Safety Data Sheet here.
Our FDA National Drug Code Number is 73855. Per FDA regulations, to report an Adverse Effect from the use of New Deal Hand Sanitizer, please fill out this form.
To use the World Health organization’s dry-rub sanitizer formula, apply liberally to hands and rub together until dry.
The World Health Organization does not recommend the addition of perfumes or other fragrances due to the risk of an allergic reaction. The active ingredient in this hand sanitizer is ethanol which does have a scent naturally produced during fermentation by yeasts and other sugars. As we have not added perfumes or fragrances the residual scent of ethanol is present, however, any odor dissipates quickly as the hand sanitizer dries.
At present, alcohol-based hand-rubs are the only known means for rapidly and effectively inactivating a wide array of potentially harmful microorganisms on hands. Currently, we have no plans to produce any sanitizer other than the World Health Organization dry-rub Formulation 1 as it was developed to have a high ethanol content, thus increasing its effectiveness. Most gel sanitizers will begin to separate past 60% ethanol while this sanitizer is stable at 80%.
Our gallon containers are standard F-style jugs with a 38-400 neck finish. Pumps can often be found through packaging distributors such as Berlin Packaging or SKS Bottle & Packaging.
The hand sanitizer we are currently manufacturing is the World Health Organization dry-rub formula 1, which is a highly-effective liquid with a watery consistency that dries very fast. Due to its consistency, if you do decide to fill smaller bottles we would recommend looking into containers with spray/atomizer tops or bottles with flip-top caps.
Dispensers can be designed to work with gel, liquid or foam sanitizers. Due to the watery consistency of this product, the most effective dispensers will be designed for liquid and built to spray rather than to distribute gel.
Hand sanitizer is classed as an over-the-counter drug and is therefore regulated by the FDA, the TTB and the Oregon Board of Pharmacy. As long as the hand sanitizer is being used in your own business (i.e. ’not for resale’) then it is permitted to refill dispensers or bottles without labeling them. The 55-gallon drum will have to be correctly labeled by the distillery and you will need to keep the SDS on file to meet OSHA requirements. According to the American Craft Spirits Association, this fulfills all of the FDA’s current labeling requirements.
Yes, our hand sanitizer has been denatured with a strong natural bittering agent. This harmless but astringent additive is to remind you that this product is not intended for consumption.
The WHO’s official recommendation is to use it within 2 years but as this product is 80% ethanol it is always going to have some microbicidal efficacy.
We have a limited amount of bulk ethanol available for purchase to those with a valid TTB permit or IAA endorsement from the OLCC.
If you have any further questions or concerns please email us at helpinghands@newdealdistillery.com or call us at (503) 234-2513
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