Origin Story
Robbie Harmon
Nutritional support reimagined. Nothing synthetic, only whole-foods, impactful dosing, and a broad array of functional ingredients to impact how your body performs.
Robbie Harmon
Tanna Fox
Kim Stoddard
Lon Henderson
Jesika Harmon
Robbie Harmon
Sarah Bega
“Since taking CORE7, I feel like a completely different person. I’m more focused and engaged, my afternoon dip vanished, my energy and resilience are better, and I’m getting the best sleep of my entire life.”
Jamie S.“With three young kids, I needed something that could actually keep up with my life. Within a few weeks of taking CORE7, I noticed more steady energy throughout the day, fewer cravings, and no longer had that same 3:00 PM crash.”
Shaelee S.“I’ve been using another all-in-one supplement for years, but after switching to CORE7, I noticed a clear difference, especially in my sleep metrics. When I went back to my old routine for a short time, I could feel the drop-off. Coming back to CORE7 made the contrast obvious.”
Eric S.“CORE7 simplifies my nutrition routine, and the biggest difference I have noticed is improved gut health, with no more bloating, better digestion, and fewer sugar cravings.”
Laurel L.“I started using CORE7 during recovery after surgery, and it quickly became part of my daily routine. My sleep is deeper and more restorative, I remember my dreams, I have more energy, and I feel so much better. I’m sold.”
Mickell W.“One of the biggest changes for me with CORE7 has been my energy later in the day. I’m still active in the evenings, playing pickleball and keeping up with everything, instead of feeling drained. Late at night I remember thinking, I could jump all over this court, I have so much energy.”
Corena H.I’m stunned by the energy I feel. I no longer hit a wall in the afternoon, and I feel more ownership of my days. At first, I thought CORE7 was just an intense multivitamin, but now I’m realizing how much it can support my mood, focus, cravings, and sleep. I am so grateful!
Emily S.“After 30 days of using CORE7, I feel like I have increased energy, less sugar cravings, and I like that I can cut back on all the different supplements. I’m excited to see where it goes from here.”
Maren B.“I track my sleep consistently, and after starting CORE7, the difference was noticeable. My sleep quality improved in a way I could actually measure, not just feel.”
Tyson T.“Switching to CORE7 helped me simplify my routine while getting the added benefits of improved gut health, increased energy, and improved mood.”
Jill A.“Since starting CORE7, my REM sleep and deep sleep are two to three times higher than they were before, my stress levels seem lower, and I feel much more calm. My sleep is so outstanding, I would take CORE7 just for the sleep benefits alone.”
Jamie S.“I love how simple CORE7 makes my routine. I used to feel so overwhelmed by all the supplements and what to prioritize, and this just makes it easy.”
Bre N.
Nutrients in forms your body naturally recognizes and uses, without synthetic isolates.
Meaningful amounts of each ingredient, formulated to deliver a noticeable impact.
Unique breadth and completeness to fill important nutrient gaps and improve how you feel every day.
Coaching, education, and wellness resources included with your subscription.
30 servings
30 servings
How Does
|
CORE7
|
AG1
|
IM8
|
|---|---|---|---|
| No Synthetics |
Only Whole Food Vitamins/ |
||
| Clinical Origins | |||
| Support Ecosystem/ |
|||
| Impactful Dosing | 20.3 g | 13.0 g | 11.8 g |
| Completeness | Illustrative Differences | Illustrative Differences | Illustrative Differences |
| Ashwagandha | 500 mg | 19th of 21 items in a 7.5 g blend | 2nd of 8 items in a 200 mg blend |
| Probiotics | 5 strains 29B CFUs | 5 strains 10B CFUs | 2 strains 10B CFUs |
| Saffron | 80 mg | ||
| Magnesium | 109 mg | 30 mg | 65 mg |
| Mushrooms |
Lion's Mane - 450mg, |
Shitake and Reishi listed 13th and 14th out of 23 items in a 1.5g blend |
Reishi, |
| Inositol | 500 mg | 100mg | |
| Omegas |
500 mg (SLA, |
||
| L-Theanine | 250 mg |
See every nutrient, blend, and Daily Value on the official label.
For your best self, naturally.
Nourishes your brain for better focus and memory while supporting long-term cognitive health.
Ahiflower® supplies ALA and stearidonic acid, a plant omega-3 that raises EPA more efficiently than ALA alone. It contains no DHA and complements—but does not replace—high-quality fish oil when direct EPA and DHA are desired.
Caronositol® provides carob-derived D-chiro-inositol for insulin signaling. Metabolic stability may indirectly support cognition, but direct evidence is limited.
L-theanine may support calm attention without sedation. Human studies suggest modest benefits for relaxation and focus, especially during demanding situations.
LP815 is a GABA-producing probiotic with emerging evidence for sleep and stress. Its brain role is gut–brain support, not direct cognitive enhancement.
Cordyceps is studied mainly for fatigue and exercise capacity, with less direct cognitive evidence. It may support clarity when fatigue is limiting.
Lion’s Mane provides compounds studied for memory and cognitive aging. Human trials are promising but limited; organic fruiting body powder offers support.
Reishi provides mushroom compounds studied for stress, fatigue, and immune function. Direct human evidence for cognition remains limited.
Turkey Tail is best studied for immune and microbiome effects, not cognition. Its brain-health contribution is indirect through the gut–immune foundation.
B vitamins support energy metabolism, methylation, and neurotransmitter synthesis. Panmol® supplies all eight in a food-based quinoa sprout matrix.
Curcuminoids support antioxidant and inflammatory-response pathways relevant to brain aging. Human cognition findings are promising but mixed and dose-dependent.
Choline supports cell membranes and acetylcholine, involved in memory and attention. VitaCholine® provides a reliable daily source.
Vitamin K2 supports calcium handling and vascular health. Its relevance to cognition is indirect, and direct memory benefits have not been established.
Supports a balanced gut and comfortable digestion, helping to reduce bloating and promote regularity.
Arrabina® is an arabinoxylan prebiotic fiber that nourishes beneficial gut bacteria and supports short-chain fatty acid production, with good human tolerability.
This plant-based enzyme blend helps break down proteins, fats, and carbohydrates. Benefits depend on the enzymes, dose, meal, and individual digestive need.
HN019 is a well-characterized probiotic studied for intestinal transit and bowel regularity. Findings are mixed, but it adds targeted Bifidobacterium support.
L-theanine may reduce perceived stress. Its role is indirect gut–brain support, not a direct digestive or microbiome effect.
LA-14 adds a well-characterized acidophilus strain supporting microbial balance. Effects remain strain-, dose-, and condition-specific.
LGG is a highly studied probiotic with strain-specific evidence for digestive resilience and gut-barrier support in defined clinical settings.
LP37 complements the probiotic blend and has been studied for stress and digestive symptoms, often within multi-strain formulas.
LP815 is studied mainly for sleep and stress. Here, it supports gut–brain communication rather than bowel regularity.
Ginger has strong human evidence for nausea, gastric motility, and digestive comfort. Organic root powder provides gingerols.
Licorice root is traditionally used for digestive comfort. Evidence depends on preparation, and whole licorice is not deglycyrrhizinated licorice.
Marshmallow root contains mucilage that can form a soothing coating. Traditional digestive use is plausible, but direct human evidence remains limited.
Saffron is better supported for mood than digestion. Its gut–brain effects are complementary; direct digestive evidence is limited.
Supports deep, restorative sleep by calming the mind and body, helping you fall asleep faster and wake feeling refreshed and energized.
Supports insulin signaling; direct sleep evidence remains limited.
Supports microbiome balance; direct evidence for sleep improvement is limited.
Supports the probiotic blend; direct evidence for sleep improvement remains limited.
LP815 has clinical evidence for sleep support through GABA-related gut–brain pathways.
Supports muscle relaxation and sleep pathways, especially when magnesium status is low.
Human studies suggest modest sleep benefits, particularly with stress or disturbed sleep.
Provides B vitamins supporting neurotransmitter pathways involved in sleep–wake regulation.
Maintains D3 adequacy, which may support sleep when levels are low.
Supports circadian and neurotransmitter processes relevant to sleep; adequacy matters most.
Fortifies your immune defenses with key nutrients and antioxidants, helping you stay healthy and resilient every day.
BioPerine® is included primarily to improve curcumin absorption, strengthening turmeric rather than acting as a major immune ingredient alone.
LGG is a highly studied probiotic with strain-specific evidence for gut-barrier support and immune–microbiome interactions.
Acerola adds naturally occurring vitamin C and polyphenols, complementing the quantified vitamin C ingredient and broadening antioxidant intake.
Blueberry contributes anthocyanins and other polyphenols that diversify antioxidant intake. Its immune contribution is supportive and indirect.
Cordyceps contains compounds studied for immune and fatigue-related effects. Human evidence for routine immune benefits from whole powder is limited.
Cranberry adds proanthocyanidins and polyphenols. Its strongest evidence concerns urinary-tract health in specific products and doses.
Pomegranate provides polyphenols that support antioxidant defenses and a healthy inflammatory response. Its immune role is supportive and indirect.
Reishi contains beta-glucans and triterpenes that interact with immune pathways. Evidence is stronger for concentrated extracts than whole powder.
Turkey Tail provides beta-glucans and polysaccharides studied for immune modulation. Evidence is strongest for standardized extracts in clinical settings.
Selenium supports antioxidant selenoproteins and normal immune and thyroid function. Benefits depend on maintaining adequate—not excessive—status.
Curcuminoids support antioxidant and inflammatory-response pathways that interact with immunity. Their role is immune balance rather than acute defense.
Vitamin A supports immune-cell differentiation and the skin and mucosal barriers. Beta-carotene provides a plant-based precursor with variable conversion.
Vitamin C supports immune-cell function and antioxidant protection. Acerola and citrus provide it within a food-derived phytonutrient matrix.
Vitamin E protects cell membranes from oxidative damage and supports normal immune signaling. Natural d-alpha tocopherol provides a dependable source.
Zinc is essential for immune-cell development, signaling, and barrier function. The bisglycinate form supports adequacy with good tolerability.
Helps convert your food into fuel to power all of your body systems, supporting a healthy metabolism for steady, all-day energy.
Calcium supports muscle contraction, nerve transmission, hormone signaling, and bone structure. Aquamin® F provides algae-derived calcium with associated trace minerals.
Caronositol® provides carob-derived D-chiro-inositol for insulin signaling. Evidence is strongest in specific insulin-resistant populations, so benefits are context-dependent.
Chromium participates in insulin action and glucose metabolism, but supplementation results are mixed. Its role is nutritional coverage, not a predictable glucose effect.
Copper supports enzymes involved in cellular energy production, iron metabolism, connective tissue, and neurotransmitter synthesis. Bisglycinate supports trace-mineral coverage.
Iodine is essential for thyroid hormones that regulate metabolic activity. Kelp provides a food-derived source; both low and excessive intake can be problematic.
Magnesium is required for ATP production, glycolysis, nerve signaling, and muscle function. Aquamin® Mg TG provides a seawater-derived source.
Manganese supports enzymes involved in carbohydrate and amino-acid metabolism, antioxidant defense, and bone formation. Its role is foundational, not stimulating.
Molybdenum supports enzymes that process sulfites and sulfur-containing compounds. Deficiency is rare, so its value is trace-mineral completeness.
B vitamins are essential cofactors that convert carbohydrate, fat, and protein into usable energy. Panmol® provides all eight without acting as a stimulant.
Potassium maintains fluid balance and electrical gradients needed for nerve transmission and muscle contraction. Effects depend on total daily dietary intake.
Selenium supports thyroid-hormone activation and antioxidant enzymes. It helps maintain metabolic adequacy but does not directly boost energy.
Choline supports cell membranes, liver fat transport, methyl-group metabolism, and acetylcholine production. VitaCholine® provides a consistent daily source.
Vitamin A supports cell differentiation, vision, immunity, and tissue maintenance. Beta-carotene provides a plant-based precursor; energy effects are indirect.
Vitamin C supports carnitine synthesis, collagen formation, and antioxidant recycling. These functions support metabolism, but vitamin C is not a stimulant.
Vitamin D supports muscle, neuromuscular, immune, and glucose-metabolism functions. Correcting low status may help fatigue; adequate levels are unlikely to boost energy.
Vitamin E protects cell membranes from oxidative damage and supports normal immune and vascular function. Its energy role is protective and indirect.
Vitamin K2 activates proteins involved in clotting and calcium handling. It complements the mineral system but does not directly produce energy.
Zinc supports hundreds of enzymes involved in protein synthesis, cell division, and metabolism. It maintains function but is not an immediate energy enhancer.
Promotes a calm, uplifted mood and sharp mental clarity, helping you stay balanced even on stressful days.
Caronositol® supports insulin signaling and cellular communication. Metabolic stability may indirectly support mood and focus, but direct evidence is limited.
L-theanine may promote calm attention and reduce acute stress without significant sedation. Human studies suggest modest benefits for relaxation and focus.
L-tyrosine is a dopamine and norepinephrine precursor. It may preserve cognition during acute stress or sleep loss; everyday mood evidence is less certain.
LP815 is a GABA-producing probiotic with emerging randomized-trial evidence for stress and sleep measures, supporting mood through the gut–brain axis.
Human studies suggest ashwagandha may modestly support perceived stress and emotional calm. Effects vary by extract and dose.
Cordyceps is studied more for fatigue than mood. It may support clarity when fatigue is limiting, but direct mental-health evidence is limited.
Small human trials suggest Lion’s Mane may support cognition and mood, but evidence remains preliminary. Organic fruiting body powder provides supportive mushroom compounds.
Reishi is traditionally used for stress and fatigue. Direct human evidence for mood benefits from whole mushroom powder remains limited.
B vitamins support energy metabolism, methylation, and neurotransmitter synthesis. Panmol® helps cover nutritional gaps that can affect mental energy and mood.
Saffron has comparatively strong clinical evidence for supporting mild-to-moderate mood symptoms. The concentrated extract supports emotional well-being without overstating the evidence.
Choline supports acetylcholine and cell membranes, contributing to normal attention and memory. VitaCholine® helps maintain adequacy; enhancement evidence is limited.
Provides a broad spectrum of nutrients from fruits and greens to fill nutritional gaps and support overall vitality.
Acerola is naturally rich in vitamin C and polyphenols. Organic powder complements the quantified vitamin C ingredient with a food-derived matrix.
Barley grass contributes chlorophyll, carotenoids, and plant compounds. Broad detox claims are unsupported, so its role is greens diversity rather than cleansing.
Beetroot supplies dietary nitrate and betalains. Human research supports nitrate-rich beet products for circulation and exercise efficiency when the nitrate dose is sufficient.
Blueberry provides anthocyanins and polyphenols studied for vascular and cognitive health. Organic powder broadens phytonutrient diversity; effects depend on dose and preparation.
Broccoli sprouts provide glucoraphanin, a precursor to sulforaphane. Conversion depends on myrosinase activity, but the pathway supports the body’s antioxidant-response enzymes.
Cranberry provides proanthocyanidins and polyphenols. Certain products and doses support urinary-tract health by reducing bacterial adhesion; whole powder adds broader phytonutrient diversity.
Ginger provides gingerols with strong evidence for nausea and digestive comfort, plus broader antioxidant activity. Organic root powder adds a clinically relevant botanical.
Kale contributes carotenoids, glucosinolates, and other plant compounds. Organic whole-leaf powder adds cruciferous diversity without replacing a serving of fresh kale.
Lemon juice powder contributes citrus flavonoids, organic acids, and flavor. Its role is broadening the fruit matrix, not delivering a clinical vitamin C dose.
Licorice root adds traditional compounds associated with digestive comfort. Evidence and safety depend on preparation and dose, so its role remains measured and supportive.
Pomegranate contributes ellagitannins and polyphenols studied for vascular and antioxidant effects. The extract adds concentrated phytonutrient diversity.
Raspberry contributes anthocyanins and ellagitannins. Organic powder broadens phytonutrient diversity without implying that it replaces whole fruit or its fiber.
Spinach contributes carotenoids, flavonoids, and micronutrients. Organic concentrate broadens food diversity but should not be presented as a full vegetable serving.
Spirulina supplies protein, minerals, carotenoids, and phycocyanin. Human benefits generally require gram-level doses, and spirulina is not a reliable active vitamin B12 source.
Sweet potato contributes beta-carotene, potassium, and food-based phytonutrients. Organic powder adds orange-vegetable diversity without replacing a whole vegetable serving.
*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.