What is the formulation and route of administration?

This product is a sterile, preservative-free preparation of oxidized NAD+ designed for intravenous administration in professional settings. It is supplied for use by licensed healthcare providers who oversee infusion setup, line checks, and observation per facility protocols. The isotonic composition supports compatibility with standard IV workflows. Refer to your internal policies for preparation steps, equipment selection, and documentation needs appropriate to your practice model.

How do clinics integrate this product into wellness or recovery services?

Facilities typically schedule supervised sessions within broader wellness menus that may include hydration and micronutrient support. Integration is shaped by each clinic’s scope of practice, staffing, and protocols for assessment, consent, and monitoring. Many teams map the infusion to existing chair capacity and rotate inventory based on predictable par levels. Session length, cadence, and follow-up are determined by clinical leadership according to local policies and professional judgment.

What are the packaging details and traceability features?

The pack is supplied as 500 mg x 1 vial with clear labeling for lot and expiration. Clinics often barcode-scan incoming units and rotate by first-expiring, first-out. The single-vial configuration simplifies reconciliation to chair usage and supports internal audits. Always verify label details upon receipt, store per packaging instructions, and document lot data in your EHR or inventory system to maintain traceability across service lines.

Who is authorized to administer IV NAD+ products in a clinic?

Administration is limited to licensed professionals operating within their state scope of practice and facility policies. Typical roles include physicians, nurse practitioners, physician assistants, and registered nurses trained in IV therapy. Clinics should also ensure that support staff follow established protocols for setup, monitoring, and documentation. Review your state regulations and institutional guidelines to confirm who may prescribe, prepare, and administer IV infusions in your facility.

How should this item be stored and handled?

Follow the storage and handling instructions on the package and product label. Maintain appropriate environmental controls, protect from contamination, and use aseptic technique during preparation and administration. Verify integrity during receiving and again at chairside. If your facility employs temperature monitoring or sealed storage, document those checks per policy. Discard any product with compromised packaging, missing data, or visible particulate inconsistent with the label.

Can it be scheduled alongside other IV therapies or nutrients?

Clinicians often consider coordinating this infusion with hydration or micronutrient protocols within the same service line. Compatibility assessments are made by the supervising provider, with attention to line selection, sequence of administration, and observation. When combining services, maintain clear documentation, prevent cross-contamination, and follow your facility’s guidance on tubing, connectors, and line flushing. Always defer to internal standards and current professional judgment for chair-level decisions.

What ordering steps are required for clinics?

Clinics need a verified account to view pricing and place orders. After credential checks, you can assign user roles, set purchasing thresholds, and align orders with your scheduling cadence. Many facilities plan monthly or biweekly replenishment cycles to maintain par levels. Ordering can also be coordinated across locations if you manage a multi-site group. Lead times may vary based on demand and allocation policies; sign in to view current availability and options.

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Pharmaceuticals

RejuvaNAD+

RejuvaNAD+ IV Infusion for Clinics

Name: RejuvaNAD+® IV Infusion – Professional Clinic Supply
SKU: 100209
Price: 259.99 USD
Availability: InStock

Injectable Medication

$259.99

Description

What RejuvaNAD+ Is and How It Works

RejuvaNAD+® is a sterile, high-purity intravenous preparation of nicotinamide adenine dinucleotide (NAD+) intended for clinical infusion protocols. It is designed for direct IV administration under professional oversight, giving clinics a consistent, reliable option for cellular-support programs. Med Wholesale Supplies serves licensed clinics and healthcare professionals with authentic, brand-name medical products sourced through vetted distributors, with US distribution to support predictable lead times.

NAD+ is a ubiquitous coenzyme involved in redox reactions and cellular energy pathways. Providing an IV formulation allows immediate systemic availability under monitored conditions. The preparation uses an oxidized NAD+ form in an isotonic vehicle suitable for infusion, produced in sterile conditions and free from added preservatives.

This product fits well in care pathways where clinical teams prioritize standard formulation, consistent handling characteristics, and dependable labeling for traceability. It can be integrated into supervised infusion menus alongside hydration and nutrient protocols, per each facility’s scope and policies. Facilities determine patient selection, workflow, and duration parameters according to their own procedures and professional judgment.

Professional Applications

Clinics use this preparation in structured infusion programs focused on cellular support, recovery services, and general wellness offerings. It may be scheduled within multidisciplinary programs that coordinate hydration, micronutrient support, and restorative care. Some facilities leverage it in intensive reset days, while others incorporate spaced sessions within broader lifestyle frameworks. Where appropriate, Pharmaceuticals from the same inventory can be aligned to streamline procurement and storage routines across service lines.

Teams often integrate RejuvaNAD+ with staff-led assessment, consent workflows, and post-session follow-ups. Education and intake protocols can be adapted to the practice model, allowing consistent expectations for clinicians and clients. For cross-disciplinary teams, the infusion may appear alongside dermatologic or regenerative offerings scheduled on separate days or in separate rooms. If your practice also explores adjunctive skin rejuvenation workflows, see our clinical read on Mesotherapy Injections for context and cross-training considerations.

Key Features

High-purity NAD+ in oxidized form suitable for IV administration
Sterile, preservative-free, isotonic formulation for professional use
Manufactured under GMP-compliant conditions with rigorous quality controls
Consistent composition to support standardized clinic protocols
Clear lot and expiration labeling for traceability
Single-vial pack configuration for straightforward inventory planning

Benefits in Practice

Many infusion services favor RejuvaNAD+ for predictable handling and straightforward scheduling. The standardized formulation helps reduce variability during preparation and improves day-to-day consistency across providers. The clear label and single-vial format simplify check-in, documentation, and stock rotation. These characteristics can help teams minimize delays at chair turnover and maintain a reliable experience across sessions.

Workflow-friendly prep: predictable setup and labeling
Staff efficiency: consistent steps reduce training time
Inventory clarity: single-vial pack aids par-level planning
Traceability: lot and expiry data support internal controls
Flexible integration: fits supervised wellness and recovery menus
Professional focus: aligns with clinic-grade infusion standards

Operationally, clinics can map the product to their safety protocols, line checks, and observation windows. Reference or adapt your internal standards around sterile handling, line integrity, and chair-side monitoring. For broader team training, review Safety Protocols to reinforce universal best practices for aseptic technique. Where your workflow includes ancillary cannula-based procedures in separate service lines, see SoftFil Cannula as a complementary option for those applications.

Composition & Ingredients

Active: Nicotinamide adenine dinucleotide (NAD+), oxidized form
Excipients: Sterile water for injections and buffering agents

The formulation is preservative-free and developed for intravenous use. Composition and excipients are intended to provide isotonicity, stability, and compatibility with standard IV administration protocols in professional settings.

Packaging & Supply

Pack configuration: 500 mg x 1 vial. Clinics typically select this configuration for predictable par-level planning and streamlined replenishment. The label includes lot and expiration data for traceability, and external packaging is designed for professional storage systems. When referencing internal inventories, use the exact pack description for clarity: RejuvaNAD+ 500 mg.

Facilities often barcode-scan incoming lots and rotate stock according to first-expiring, first-out principles. The single-vial format is also straightforward for audit trails and for reconciling chair usage to inventory. Strength reference appears on the primary packaging; verify all label details as part of your receiving checklist.

Ordering & Logistics

Access is limited to licensed clinics and healthcare facilities with verified accounts. Sign in to view contract and volume tiers. If your organization requires purchase controls, assign user roles and approval limits within your account to streamline internal ordering steps. Most clinics align ordering windows with clinic schedules to ensure appropriate on-hand quantity.

When onboarding, our team can help consolidate similar items into a unified purchasing plan. This reduces time spent across vendors and supports coordinated replenishment. For guidance on sourcing related devices and accessories, see How To Buy Cannulas for procurement tips that easily translate to infusion inventory planning.

Comparable Products

For clinics that also offer regenerative or biostimulatory skin procedures, consider pairing your infusion menu with adjunctive injectables selected for tissue support in separate appointments. Options from our catalog include Nucleofill 20 and Polynucleotide Gel. These products serve different indications than an IV NAD+ preparation, but many practices stock them together to build cohesive wellness and aesthetic programs under one supply chain.

Pricing & Access

Sign in to view current availability and tiers, including volume and contract pricing structured for clinical procurement. RejuvaNAD+ is reserved for licensed accounts; onboarding includes verification of credentials and facility details. Multi-location groups can coordinate centralized purchasing or site-level access, depending on how you manage formularies and service lines. For larger commitments, our team can discuss scheduled releases that match clinic calendars.

Availability & Substitutions

Supply can vary based on production cycles and regional demand. If an item is temporarily unavailable, our team can help identify suitable alternatives from your approved formulary list, with consideration for formulation characteristics and workflow fit. Confirm substitutions with your clinical leadership before use. Backorders, if any, are managed on a first-come basis at the time of allocation.

Authoritative Sources

Ready to align your inventory? Our team can help schedule procurement that fits your clinic calendar, with temperature-controlled handling when required and tracked US delivery.

Frequently Asked Questions

What is the formulation and route of administration?
This product is a sterile, preservative-free preparation of oxidized NAD+ designed for intravenous administration in professional settings. It is supplied for use by licensed healthcare providers who oversee infusion setup, line checks, and observation per facility protocols. The isotonic composition supports compatibility with standard IV workflows. Refer to your internal policies for preparation steps, equipment selection, and documentation needs appropriate to your practice model.
How do clinics integrate this product into wellness or recovery services?
Facilities typically schedule supervised sessions within broader wellness menus that may include hydration and micronutrient support. Integration is shaped by each clinic’s scope of practice, staffing, and protocols for assessment, consent, and monitoring. Many teams map the infusion to existing chair capacity and rotate inventory based on predictable par levels. Session length, cadence, and follow-up are determined by clinical leadership according to local policies and professional judgment.
What are the packaging details and traceability features?
The pack is supplied as 500 mg x 1 vial with clear labeling for lot and expiration. Clinics often barcode-scan incoming units and rotate by first-expiring, first-out. The single-vial configuration simplifies reconciliation to chair usage and supports internal audits. Always verify label details upon receipt, store per packaging instructions, and document lot data in your EHR or inventory system to maintain traceability across service lines.
Who is authorized to administer IV NAD+ products in a clinic?
Administration is limited to licensed professionals operating within their state scope of practice and facility policies. Typical roles include physicians, nurse practitioners, physician assistants, and registered nurses trained in IV therapy. Clinics should also ensure that support staff follow established protocols for setup, monitoring, and documentation. Review your state regulations and institutional guidelines to confirm who may prescribe, prepare, and administer IV infusions in your facility.
How should this item be stored and handled?
Follow the storage and handling instructions on the package and product label. Maintain appropriate environmental controls, protect from contamination, and use aseptic technique during preparation and administration. Verify integrity during receiving and again at chairside. If your facility employs temperature monitoring or sealed storage, document those checks per policy. Discard any product with compromised packaging, missing data, or visible particulate inconsistent with the label.
Can it be scheduled alongside other IV therapies or nutrients?
Clinicians often consider coordinating this infusion with hydration or micronutrient protocols within the same service line. Compatibility assessments are made by the supervising provider, with attention to line selection, sequence of administration, and observation. When combining services, maintain clear documentation, prevent cross-contamination, and follow your facility’s guidance on tubing, connectors, and line flushing. Always defer to internal standards and current professional judgment for chair-level decisions.
What ordering steps are required for clinics?
Clinics need a verified account to view pricing and place orders. After credential checks, you can assign user roles, set purchasing thresholds, and align orders with your scheduling cadence. Many facilities plan monthly or biweekly replenishment cycles to maintain par levels. Ordering can also be coordinated across locations if you manage a multi-site group. Lead times may vary based on demand and allocation policies; sign in to view current availability and options.

Specifications

Main Ingredient:
Manufacturer: Penmix Co., Ltd.
Drug Class: Medical Device
Generic Name: Nicotinamide adenine dinucleotide (NAD⁺)
Package Contents: 500 mg x 1 Vial
Storage Requirements: Room Temperature (2℃~25℃)
Main Usage:

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