
This intranasal formulation delivers NAD+ directly through your nasal passages into your bloodstream and brain. Feel the difference in your energy, mental clarity, and recovery — at the cellular level.
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Individual results may vary. Benefits described are based on clinical and pharmacological evidence and do not constitute a guarantee of treatment outcomes. All treatment requires evaluation and approval by a licensed provider.




NAD Nasal Spray is a prescription therapy used for cognitive and energy support.
Patients seeking support for cognitive and energy support may qualify after evaluation by a licensed provider.
Yes. This is a compounded intranasal preparation requiring a valid prescription from a licensed provider.
Mild nasal irritation, congestion, or transient flushing are the most commonly reported effects. Some patients report a brief sensation of warmth or mild headache following administration, consistent with effects commonly reported with NAD+ administration. These effects are generally short-lived.
Patients with known hypersensitivity to nicotinamide or NAD+ components should not use this product. Patients with active malignancy should consult their oncologist before use, as NAD+ supports cellular proliferation pathways including PARP and sirtuin activity. Use during pregnancy or breastfeeding requires provider evaluation.
NAD+ does not have established clinically significant drug interactions at therapeutic intranasal doses. Concurrent use of PARP inhibitors (e.g., olaparib) used in oncology may reduce the efficacy of either agent; patients on PARP inhibitor therapy should consult their oncologist before use.
Patients with a history of hormone-sensitive or proliferative malignancy require oncological clearance before initiating NAD+ therapy given its role in cellular energy and repair pathways. Patients with severe hepatic impairment should discuss use with their provider. Routine monitoring is not required in otherwise healthy patients.
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