Self-administer in seconds. Within weeks, patients report sharper focus, faster recovery, and energy that holds through the afternoon.
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NAD+ is the molecule your cells use to convert food into ATP — the energy currency that powers every breath, every thought, every muscle contraction. It's also the fuel for two repair systems that keep you young: sirtuins (longevity proteins) and PARPs (DNA repair).
By age 40, your cells produce NAD+ slower than they consume it. By age 60, systemic levels can fall by 50%. This shortage creates a state called "pseudohypoxia" — your cells behave as if they're oxygen-starved, even when they're not. Mitochondrial communication breaks down. Genomic repair slows. The visible markers of aging — fatigue, weight gain, slower recovery, thinner skin, cognitive fog — emerge.
Restoring NAD+ doesn't just refill a tank. It reactivates the entire metabolic network that depends on it — sirtuins that protect mitochondria, PARPs that repair DNA, and the signaling pathways that orchestrate cellular renewal. It's why patients consistently report feeling "the version of themselves from 10 years ago."
High-energy tissues — brain, heart, muscle, skin — are the first to feel the depletion and the first to feel the restoration.
NAD+ restoration reduces beta-amyloid plaque formation and rebuilds neuronal mitochondrial morphology. Patients report sharper thinking, better memory recall, and reduced afternoon brain fog within weeks.
Activates the SIRT1/SIRT3-mediated mitochondrial unfolded protein response, improving insulin sensitivity and oxygen utilization. Translates to easier weight management and sustained energy.
Rejuvenates muscle stem cells through the Sirt1-PGC-1α axis. Restores mitochondrial signaling needed for strength, endurance, and faster post-workout recovery.
Inhibits MMP-1 collagen breakdown, repairs UV-induced DNA damage, and reduces cellular senescence. The "Inside-Outside" approach modern dermatology now considers foundational.
Directly supports Complex I of the electron transport chain — the gatekeeper of ATP production. Cellular energy without the crash of caffeine or stimulants.
Counters the CD38-driven inflammatory "sink" that aggressively degrades NAD+ with age. Restoring balance shifts the body from chronic inflammation toward repair.
No clinic visit. Complete a medical questionnaire — a board-certified physician reviews your protocol — your NAD+ ships from a US-licensed compounding pharmacy.
Medical Questionnaire
Complete a brief intake from home. Five minutes — covers medical history, current medications, and your goals.
Physician Review
A board-certified physician reviews your protocol within 24 hours. Reaches out if anything needs clarifying.
Compounded & Shipped
US-licensed pharmacy compounds your NAD+ and ships overnight in temperature-controlled packaging.
Self-Administer
Subcutaneous injection at home, 2–3x per week per protocol. Includes detailed instructions and provider access for questions.
Individual results vary based on baseline NAD+ levels, age, and protocol. These are the most consistent patterns we observe.
Earliest patient reports describe sharper focus and increased bioenergetic capacity — particularly in the afternoons when energy typically dips.
Quantifiable increases in blood NAD+ and NAAD biomarkers. Energy stabilizes throughout the day. Sleep quality improves for most patients.
Insulin sensitivity improvements, increased muscle recovery rate, dermatological brightness, and reduced markers of inflammaging emerge as the cellular repair systems reach full activity.
Once peak restoration is achieved, your provider adjusts dosing for long-term maintenance. Many patients continue indefinitely as part of a longevity protocol.
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For patients who want to understand why physician-supervised NAD+ replenishment outperforms over-the-counter supplements.
Your cells primarily make NAD+ by recycling Nicotinamide (NAM) through the rate-limiting enzyme NAMPT. Aging slows this pathway — supplementing with NR or NMN bypasses the bottleneck.
NMNAT enzymes that finalize NAD+ synthesis exist in three forms: NMNAT1 (nucleus), NMNAT2 (cytosol/Golgi), and NMNAT3 (mitochondria). Effective therapy must serve all three compartments.
SIRT1, SIRT3, and SIRT6 are NAD+-dependent. When NAD+ is scarce, sirtuins shut down — directly compromising mitochondrial health, DNA repair, and stem cell rejuvenation.
Every time UV light or oxidative stress damages your DNA, PARP1/2 jump in to repair it. They consume massive amounts of NAD+ — chronic damage can deplete 50% of cellular NAD+ alone.
This enzyme expands with chronic inflammation and aggressively hydrolyzes both NAD+ and its precursors. Inflammaging creates a metabolic sink that physician-supervised therapy works to counter.
A sensitive indicator of increased NAD+ synthesis. Subcutaneous and IV protocols rapidly elevate this marker — measurable proof your cells are converting the molecule into active cofactor.