PEP-NAD-500-MG • RESEARCH USE ONLY

NAD+ (500 mg)

A critical coenzyme for cellular energy production and DNA repair, supplied as a 500 mg lyophilized vial for subcutaneous injection. Supports mitochondrial function, cognitive performance, and healthy aging.

500 mg

Per Bottle
Reconstituted to 100 mg/mL

>99%

Purity
Third-party verified

Injectable

Format
Subcutaneous injection
Protocol & Dosing

Administer subcutaneously, daily or several times weekly depending on energy and cognitive needs. Individuals sensitive to stimulatory effects may prefer morning-only dosing. NAD+ can be taken with or without food; however, individuals who experience mild nausea or warmth may find it more comfortable to use with a small meal. Safe for long-term use, though taking 1 week off every 8–12 weeks may optimize receptor and mitochondrial responsiveness.

Standard
50–100 mg (50–100 units)
Medium
100–200 mg (100–200 units)
Higher
200–300 mg (200–300 units)
Cycles
  • May be used daily or several times weekly for 8–12 weeks
  • Take 2–4 weeks off every 8–12 weeks to optimize mitochondrial responsiveness, especially if stacking multiple mitochondrial compounds like MOTS-C and SS-31
Key Benefits

Boosts energy and endurance at the cellular level

Improves mental clarity, focus, and cognitive performance

Enhances mitochondrial function and ATP production

Supports metabolic health and healthy weight management

Accelerates recovery and reduces fatigue & burnout

Promotes healthy aging and cellular repair

Enhances detoxification pathways

Guidance
  • Administer subcutaneously; rotate injection sites to reduce irritation
  • Increase dosing gradually based on energy and cognitive response
  • Weekly total typically ranges 200–600 mg, dosed 1–3× weekly or daily
  • Individuals sensitive to stimulatory effects may prefer morning-only dosing
  • May be taken with or without food; those prone to mild nausea or warmth may prefer taking with a meal
  • Refrigerate reconstituted vial; use within the stability window
  • Ideal for energy, cognition, metabolic resilience, and longevity support
  • Non-hormonal and well tolerated
  • Pairs well with MOTS-C, SS-31, and Humanin for comprehensive mitochondrial support
INJECTABLE DELIVERY FORMAT

Subcutaneous Injection Protocol

NAD+ is supplied as a 500 mg lyophilized vial for reconstitution and subcutaneous administration — a shift from the nasal spray format used by other Zenith Nano™ peptides. Reconstituted to 100 mg/mL with bacteriostatic water, each vial is manufactured under cGMP conditions with full third-party verification and batch-level traceability.

Reconstitution protocol
Add 5 mL (500 units on an insulin syringe) of bacteriostatic water to the vial and gently swirl until fully dissolved — do not shake. This yields a final concentration of 100 mg/mL, where 1 mg NAD+ = 0.01 mL = 1 unit on an insulin syringe.
Storage & stability
Refrigerate the reconstituted vial and use within the stability window to preserve potency.
Injection guidance
Administer subcutaneously and rotate injection sites to reduce irritation. Dosing may be increased gradually based on energy and cognitive response.
Dosing precision
A concentration of 100 mg/mL means 1 mg = 0.01 mL = 1 unit on a standard insulin syringe, allowing precise titration across standard, higher therapeutic, and intensive protocols.
Quality assurance
Third-party COAs from AxisPharm LLC confirm full LCMS identity, >99% purity, and LAL endotoxin testing, with net peptide mass verified and batch-level traceability.
Synergistic pairings
Complements other longevity peptides — MOTS-C, SS-31, and Humanin — for comprehensive mitochondrial support.

Compliance · Zenith Nano™ Peptides

cGMP manufacturing & cryopreservation

Manufactured through Pacific Manufacturing & Design LLC — GMP-certified under NSF/ANSI 455-2 and FDA-registered (Reg. No. 15492349536). Compliant with 21 CFR Parts 11, 111, and 117. Strict quality control, validated processes, and full traceability from raw material to final product.

NSF/ANSI 455-2FDA REGISTERED21 CFR PART 11121 CFR PART 117
Third-Party COA — Every Batch

Third-party COA for every batch, ensuring consistent quality and purity. Verified through LCMS and endotoxin testing, with full traceability from raw material to final product.

LCMS CONFIRMED>99% PURITYENDOTOXIN TESTEDAXISPHARM COA