HOW DOES MUSCALARPRO™ WORK?
[M3] 3 Molecule Stack the cellular firmware that decodes peak performance
CELLULAR DECLINE
Peak performance is biological code, but cellular firmware degrades, affecting strength, endurance, and cognition.
MUSCALARPRO™ [M3]
The firmware update that rewires your cellular engine through mitophagy, autophagy, and Nrf2 antioxidant defense.
RESULTS
Sustained power output, increased muscle strength, and mental edge — delivered at the cellular level.*
The Ultimate Muscle Powerhouse
![[M3]](/_next/image?url=https%3A%2F%2Fcdn.shopify.com%2Fs%2Ffiles%2F1%2F0668%2F1486%2F9571%2Ffiles%2FMuscalarpro_capsule.png%3Fv%3D1770369222&w=3840&q=75) [M3] |  CoQ10 |  Creatine |  Leucine |  NMN | |
|---|---|---|---|---|---|
| Musclespan (strength + endurance) | Partial | Partial | Limited | ||
| Directly activates mitophagy | Partial | ||||
| Targets a root cause of age-related cellular energy decline | Partial | Partial | Partial | ||
| Benefits without exercise | |||||
| Nootropic and cognitive effects | Partial | Partial | Limited | Partial | Limited |
| Complete human clinical trials | Limited | Limited |
Mitochondrial renewal increases by +39% after 16 weeks over placebo*
Rigorously tested and made from high-quality ingredients
We believe that it's our responsibility to take the extra steps necessary to ensure that our products are safe and effective, and we are committed to upholding these high standards for all of our dietary supplements.
Every batch of M3 is screened for heavy metals, pesticide residues, residual solvents, and allergens through independent third-party laboratories. We test what you can't see — because what's not in the capsule matters as much as what is.
HEAVY METALS
Lead, Arsenic, Cadmium, Mercury
PESTICIDE RESIDUES
Multi-residue screening panel (400+ compounds)
RESIDUAL SOLVENTS
Class 1, 2, and 3 solvent analysis per ICH Q3C
ALLERGENS
Gluten, soy, dairy, shellfish, tree nut screening
Reference: USP <232> / <233> Elemental Impurities · ICH Q3D · FSSAI heavy metal limits
Microbial contamination is a silent risk in supplement manufacturing. Every M3 batch is tested for total microbial count, yeast, mold, and specific pathogens — ensuring what you ingest is biologically clean at the colony-forming unit level.
TOTAL AEROBIC COUNT
TAMC — Total Aerobic Microbial Count (<1,000 CFU/g)
YEAST & MOLD
TYMC — Total Yeast and Mold Count (<100 CFU/g)
PATHOGEN PANEL
Salmonella, E. coli, Staphylococcus aureus, Pseudomonas
ENDOTOXIN
Bacterial endotoxin screening (LAL method)
Reference: USP <61> / <62> Microbiological Examination · FSSAI microbiological limits for dietary supplements
M3 is screened for 300+ prohibited substances per WADA anti-doping protocols — including anabolic steroids, stimulants, beta-2 agonists, diuretics, and masking agents. If you compete, or even if you don't — you deserve to know your supplement is clean.
ANABOLIC AGENTS
Steroids, SARMs, prohormones, peptide hormones
STIMULANTS
Amphetamines, ephedrine, DMAA, synephrine, caffeine analogs
BETA-2 AGONISTS
Clenbuterol, salbutamol, formoterol
MASKING AGENTS
Diuretics, probenecid, plasma expanders
Reference: WADA Prohibited List 2025 · NSF/ANSI 173 Dietary Supplement Standard · Informed Sport / Informed Choice testing framework
What's in the capsule on Day 1 must still be there on Day 730. Every M3 formulation undergoes both accelerated and real-time stability testing under controlled temperature and humidity conditions — ensuring potency, purity, and physical integrity from manufacturing through expiration.
ACCELERATED STABILITY
40°C / 75% RH for 6 months — simulates 2 years of shelf conditions in 6 months
REAL-TIME STABILITY
25°C / 60% RH for 24 months — actual long-term storage monitoring
PARAMETERS TESTED
Assay, dissolution, moisture content, color, odor, disintegration time
DEGRADATION PRODUCTS
Breakdown compound monitoring — no harmful degradants at shelf life endpoint
Reference: ICH Q1A(R2) Stability Testing of New Drug Substances · WHO Technical Report Series stability guidelines · FSSAI shelf-life requirements for dietary supplements
What's on the label must be in the capsule. Every batch of M3 undergoes quantitative potency analysis of all three active/marker compounds — confirming that Urolithin A, Spermidine, and S-Allyl Cysteine meet or exceed the stated label claim. No underdosing. No asterisks.
UROLITHIN A ASSAY
Punica Granatum Extract standardized to Urolithin A — verified ≥500mg per capsule (1,000mg per serving)
SPERMIDINE ASSAY
Wheat Germ Extract standardized to Spermidine — verified ≥3mg per capsule (6mg per serving)
SAC ASSAY
Allium Sativum Extract standardized to S-Allyl Cysteine — verified ≥0.5mg per capsule (1mg per serving)
LABEL CLAIM VERIFICATION
Batch certificate of analysis (CoA) issued per lot — available on request
Reference: USP <621> Chromatography · ICH Q2(R1) Analytical Validation · 21 CFR Part 111 (cGMP for dietary supplements — identity, purity, strength, composition)
10+ placebo-controlled clinical studies
For over 15 years, we have built on meaningful scientific discoveries across Urolithin A, Spermidine, and S-Allyl Cysteine and put them to the scrutiny of the scientific community by publishing in high-impact, peer-reviewed journals.
Muscle Strength
RCT in overweight adults aged 40–64, 16-week supplementation at 1,000mg. Significant improvement in hamstring muscle strength measured via knee flexion and extension dynamometry.
Peak VO₂ Max
In sedentary, overweight 40–64 year olds, 16 weeks of 1,000mg Urolithin A produced measurable improvements in aerobic capacity without any change in exercise regimen — suggesting direct mitochondrial efficiency gains.
Brain Health
Urolithin A activated PINK1/Parkin mitophagy in neuronal cells, clearing dysfunctional mitochondria that accumulate in brain tissue with age. Pre-clinical models showed reduced neuroinflammation markers and improved synaptic signaling in hippocampal tissue.
Mitochondrial Health
1,000mg Urolithin A activated phosphorylated Parkin (Ser65) in human skeletal muscle, increasing mitophagy flux by 39% over placebo at 16 weeks. OXPHOS protein expression in skeletal muscle biopsies confirmed biogenesis of new, functional mitochondria with improved electron transport chain efficiency.
