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Mitochondrial Formula, 72g Powder

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Mitochondrial Formula is a unique combination of nutrients designed to enhance mitochondrial function and energy by increasing ATP production, while also providing intracellular antioxidant protection. Stimulant-free


    • Nutrients - amino acids, antioxidants
    • Energy - cognition, memory, athletic performance
    • Longevity - cardiovascular health, migraine

      Feature Ingredients

      • Provides a high dose of clinically relevant amounts of key nutrients, including 300 mg of CoQ10 and 1500 mg of Acetyl-L-carnitine
      • Contains a combination of ancient peat and apple extracts shown to increase ATP levels, the primary currency of cellular energy, without increasing reactive oxygen species
      • Antioxidant protection from superoxide dismutase and OpitacTM L-glutathione provides redox balance within the cell

          Mitochondria are the energy powerhouses of the cell, consuming 80–90% of a cell’s oxygen to produce ATP via the oxidative phosphorylation (OXPHOS) process. Impaired mitochondrial bioenergetics underly both the aging process and many chronic cardiovascular, metabolic, and neurological conditions.1

          • Acetyl-L-carnitine shuttles fatty acids across the mitochondrial membrane, essential for generating energy via fatty acid metabolism. It has been shown to improve fatigue, neurological and cognitive function, and blood pressure.2, 3, 4, 5
          • The antioxidant CoQ10 is a component of the mitochondrial respiratory chain and an essential cofactor in the electron transport system. It has shown clinical benefit form any conditions, including hypertension and migraine.6
          • ElevATP™ is a blend of plant bio-inorganic trace minerals and an apple extract rich in polyphenols such as rocyanidins and chlorogenic acid. It has been shown to increase whole blood ATP levels as well as exercise performance and body composition, without an increase in reactive oxygen species.7, 8, 9, 10
          • Given that mitochondria are the primary source of free radical production within a cell, the bioavailable OpitacTM L-glutathione and superoxide dismutase (from Extramel®) are also key components. They are critical to redox balance within a cell and have been shown to reduce perceived stress and fatigue.11, 12, 13

              Serving Size: 1 Heaping Scoop (2.4 g)

              Servings per Container:  30

              Medicinal Ingredients

              Each Serving (1 heaping scoop = 2.4 g) Contains:
              Acetyl-L-carnitine (N-acetyl L-carnitine hydrochloride) 1500 mg
              Coenzyme Q10 (microorganism) 300 mg
              ElevATPTM 150 mg
              Ancient Peat Extract 148.5 mg
              Apple Extract 85:1 (Malus domestica) (fruit) 1.5 mg
              OpitacTM L-glutathione 100 mg
              Cucumis melo subsp. melo var. cantalupo (fruit) 2 mg
              Superoxide Dismutase 140 IU
              (from 10 mg Extramel®)

              Non-Medicinal Ingredients

              Shellac gum, natural watermelon flavour, purified stevia leaf extract.


              Contains No Added: artificial colours, preservatives, or sweeteners; dairy, sugar, wheat, gluten, soy, corn, egg, fish, shellfish,  salt, tree nuts, or GMOs.  Suitable for Vegetarians.

              Recommended Use

              Adults 19+: 1 heaping scoop (2.4 g) per day dissolved in 250 ml of water or as directed by a health care practitioner. Take with food. Ensure you drink enough fluid before, during, and after exercise. Use a minimum of 4 weeks to see beneficial effects.

              Bioclinic Naturals Advantage

              Highly bioavailable ingredients for optimal absorption.


              Do not use if you are hypersensitive or allergic to any of the ingredients.


              Consult a health care practitioner prior to use if you are taking any medications, or if you have any pre-existing condition.  Discontinue this product 2 weeks prior to surgery.

              While no specific contraindication exists or is predicted, data is lacking for use during pregnancy, lactation, and in children, and the dosage may need to be reduced for those under the age of 18.

              Although very little evidence supports this interaction, a potential interaction is possible for those taking the anticoagulant Coumadin and both CoQ10 and acetyl-l-carnitine. Close monitoring of the INR is recommended in these patients. No other negative drug interactions are known for CoQ10, though a number of medications inhibit CoQ10 synthesis or function in the body, including statin or blood pressure medications, tricyclic antidepressants, and oral hypoglycemic agents, suggesting a potential benefit of combined use.

              Side Effect Risks

              Discontinue use and consult a healthcare practitioner if symptoms persist, worsen or you develop any reactions which may include: allergy or intolerance.  Keep out of reach of children. Sealed for your protection. Do not use if seal is broken. For freshness, store in a cool, dry place.


              The information and product descriptions that appear on this website are for information and educational purposes only and are not intended to provide or replace medical advice to individuals from qualified health care professionals. Consult your physician if you have any health concerns, and before initiating any new dietary, exercise, supplements or other lifestyle changes.


                1. Paradies G, Paradies V, Ruggiero FM, et al. Mitochondrial bioenergetics decay in aging: beneficial effect of melatonin. Cell Mol Life Sci. 2017; 74(21):3897-3911.
                2. Ruggenenti P, Cattaneo D, Loriga G, et al. Ameliorating hypertension and insulin resistance in subjects at increased cardiovascular risk: effects of acetyl-L-carnitine therapy. Hypertension. 2009; 54(3):567-574.
                3. Malaguarnera M, Gargante MP, Cristaldi E, et al. Acetyl L-carnitine (ALC) treatment in elderly patients with fatigue. Arch Gerontol Geriatr. 2008; 46(2):181-190.
                4. Sima AA, Calvani M, Mehra M, et al. Acetyl-L-carnitine improves pain, nerve regeneration, and vibratory perception in patients with chronic diabetic neuropathy: an analysis of two randomized placebo-controlled trials. Diabetes Care. 2005; 28(1):89-94.
                5. Wang SM, Han C, Lee SJ, et al. A review of current evidence for acetyl-l-carnitine in the treatment of depression. J Psychiatr Res. 2014; 53:30-37.
                6. Littarru GP, Tiano L. Clinical aspects of coenzyme Q10: an update. Curr Opin Clin Nutr Metab Care. 2005; 8(6):641-646.
                7. Reyes T, Nemzer B, Argumedo R, et al. Effect of the dietary supplement ElevATP on blood ATP level: An acute pilot clinical study. J Aging Res Clin Pract. 2013; (2):178-184.
                8. Reyes-Izquierdo T, Nemzer B, Argumedo R, et al. The effect of ElevATPTM on exercise output: a single dose, blinded, three-way cross-over study. Curr Trends Nutraceut. 2016; 1(2): 1-9.
                9. Joy JM, Vogel RM, Moon JR, et al. Ancient peat and apple extracts supplementation may improve strength and power adaptations in resistance trained men. BMC Complement Altern Med. 2016; 16:224.
                10. Joy JM, Falcone PH, Vogel RM, et al. Supplementation with a proprietary blend of ancient peat and apple extract may improve body composition without affecting hematology in resistance-trained men. Appl Physiol Nutr Metab. 2015; 40(11):1171-1177.
                11. Quintana-Cabrera R, Bolaños JP. Glutathione and ?-glutamylcysteine in the antioxidant and survival functions of mitochondria. Biochem Soc Trans. 2013; 41(1):106-110.
                12. Honda Y, Kessoku T, Sumida Y, et al. Efficacy of glutathione for the treatment of nonalcoholic fatty liver disease: an open-label, single-arm, multicenter, pilot study. BMC Gastroenterol. 2017; 17(1):96.
                13. Carillon J, Notin C, Schmitt K, et al. Dietary supplementation with a superoxide dismutase-melon concentrate reduces stress, physical and mental fatigue in healthy people: a randomised, double-blind, placebo-controlled trial. Nutrients. 2014; 6(6):2348-2359.