PEA Relief™

Palmitoylethanolamide (PEA) with full-spectrum hemp extract

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PEA has been shown to support bodily comfort and increase subjective measures of quality of life. Patent-pending PEA Relief is a unique blend of palmitoylethanolamide (PEA) and organic, full-spectrum hemp oil extract shown in a preclinical study to enhance the presence of PEA in the blood circulation.*

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Supplement Facts
Serving size: 1 softgel
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Benefits of PEA

PEA, a bioactive lipid molecule that the body produces naturally in response to noxious stimuli, can also be found in lipid extracts of plants and vegetables such as soybean lecithin and many more.1 PEA has been researched for over 70 years and has a wide range of clinical applications from mild discomfort and immune system support to mood and neurological health.*

Bodily discomfort
Bodily discomfort

Clinical evidence supports the application of PEA in relieving occasional bodily discomfort.*

Neurological health
Neurological health

Preclinical studies have indicated PEA helps support neurological health by supporting healthy mood, cognitive functions, and motor function.*

Immune system
Immune system

PEA supports the healthy function of immune cells.*2,3

1. Iannotti FA et al. Prog Lipid Res. 2016;62:107-128.
2. Gabrielsson L et al. Br J Clin Pharmacol. 2016;82(4):932-942.
3. Paladini A et al. Pain Physician. 2016;19(2):11-24.

Hemp extract

Hemp extract

Hemp extract consists of a wide range of naturally occuring beneficial phytocannabinoids, terpenes, and other plant compounds.4,5 The full-spectrum hemp oil in PEA Relief contains a custom blend of phytocannabinoids, naturally occurring terpenes, and terpenes from black pepper and cloves.

4. Russo EB. Br J Pharmacol. 2011;163(7):1344-1364.
5. Andre CM et al. Front Plant Sci. 2016;7:19.

Terpenes

Terpenes are fragrant oils naturally present in many plants and spices, including citrus fruit rinds, mango, thyme, black pepper, peppermint, to name just a few.6 These molecules are known to carry a wide array of beneficial properties.*

6. Russo EB. Trends Pharmacol Sci. 2016;37(7):594-605.

Terpenes
Hemp entourage effect

Prolonged relief

In a preclinical study, the unique combination of PEA with a proprietary, organic, full-spectrum hemp extract prolonged the presence of PEA in the body.*

What is the endocannabinoid system (ECS)?

The ECS is a regulatory system within the body that plays a role in various health aspects. The ECS consists of receptors, endogenous cannabinoids (known as endocannabinoids), and their metabolic enzymes.7,8 Endocannabinoids are “messengers,” produced and released on demand from the brain and peripheral tissues and activate their targets only when and where needed.7,8

7. Aizpurua-Olaizola O et al. Drug Discov Today. 2017;22(1):105-110.
8. Di Marzo V et al. Nat Rev Drug Discov. 2004;3(9):771-784.

Why choose ours?

We don’t care about doing it first; we care about doing it right. With so many hemp products on the market, choosing the best one isn’t easy. That’s why we’ve worked hard to bring you a high-quality, full-spectrum hemp extract you can trust—without all the guesswork.

But don’t take our word for it. See exactly what’s in your formula, with TruQuality.

Learn More
Compare our hemp formulas
Hemp Oil
Formula
Form
Non-GMO
Organic hemp extract
Glyphosate-tested
Phytocannabinoids
Exclusive hemp extract blend
Added terpenes
PEA
Patent pending
Liquid dropper
 
 
 
 
PEA Relief
Formula
Form
Non-GMO
Organic hemp extract
Glyphosate-tested
Phytocannabinoids
Exclusive hemp extract blend
Added terpenes
PEA
Patent pending
Softgel

Resources

Patient Brochure

Patient Brochure

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Endocannabinoid System FAQ

Endocannabinoid System FAQ

Download
PEA Relief Formula Focus Sheet

Formula Focus Sheet

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References

1. Iannotti FA et al. Prog Lipid Res. 2016;62:107-128.
2. Gabrielsson L et al. Br J Clin Pharmacol. 2016;82(4):932-942.
3. Paladini A et al. Pain Physician. 2016;19(2):11-24.
4. Russo EB. Br J Pharmacol. 2011;163(7):1344-1364.
5. Andre CM et al. Front Plant Sci. 2016;7:19.
6. Russo EB. Trends Pharmacol Sci. 2016;37(7):594-605.
7. Aizpurua-Olaizola O et al. Drug Discov Today. 2017;22(1):105-110.
8. Di Marzo V et al. Nat Rev Drug Discov. 2004;3(9):771-784.

 

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