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AUREVIA CD//FLOW

Final combined fill volume [pending] · Pack imagery represents current concept and is subject to change.

AUREVIA CD · Practitioner System

AUREVIA CD//FLOW

Practitioner circulation system for endothelial wellness, nitric oxide and fibrinolytic balance.

Development CollectionPractitioner Formulation Candidate. Ingredient-level research across nitric-oxide, endothelial and fibrinolytic literature. Finished-product studies pending. Ingredients, quantities, serving instructions and commercial claims remain subject to change.
Practitioner SystemDualPhase™ SystemSunflower phospholipids · cholesterol-free

AUREVIA CD//FLOW pairs HPβCD in a citrulline-forward aqueous matrix with a phyto-active phospholipid phase carrying nattokinase, beetroot and pine bark extracts. The formulation is designed for practitioner-guided use in adults seeking targeted circulation, endothelial and fibrinolytic-balance support.

$196$224Member price· 30 dual-chamber liquid-gel sachets

Not available for purchase until finished-product validation is complete.

DualPhase™ architecture
Separated during storage
Analytical validation programme
Transparent formulation
AUREVIA DualPhase™ System

Cyclodextrin intelligence. Liposomal precision.

Each daily unit contains two connected chambers — a purified aqueous cyclodextrin matrix and a separately manufactured phospholipid phase — combined only at the moment of use.

Phase One — Citrulline Matrix

  • HPβCDPending regulatory & safety review
    • Advanced cyclodextrin-research component
    • Analytical inclusion platform
  • L-Citrulline
    • Nitric-oxide precursor pathway
    • Endothelial wellness positioning
    • Practitioner-guided circulation support
  • Purified water · vegetable glycerin · buffer system
    • Aqueous carrier, viscosity, palatability and stability

Phase Two — Phyto-Active Delivery

  • Nattokinase (verified activity units)
    • Fibrinolytic-balance research relevance
    • Practitioner-guided circulation support

    Do not use with anticoagulant or antiplatelet medication unless specifically approved by the prescribing clinician.

  • Standardised beetroot extract
    • Dietary nitrate contribution
    • Vascular-wellness positioning
  • Pine bark extract (standardised OPCs)
    • Polyphenol antioxidant
    • Endothelial-wellness research relevance
  • Sunflower phosphatidylcholine
    • Cholesterol-free liposomal carrier
    • Disperses lipid-compatible phyto-actives
  • Natural mixed tocopherols
    • Oxidative protection of the phospholipid phase
DisclosureCyclodextrin inclusion is dynamic, reversible and concentration-dependent. The AUREVIA DualPhase™ System is designed to reduce prolonged cyclodextrin–phospholipid contact before use and to preserve a measurable free or exchangeable cyclodextrin fraction. This must be demonstrated through finished-product analytical testing.
Proposed consumer positioning

Designed to support.

Proposed structure/function positioning. Requires final formulation-specific substantiation and regional regulatory approval.

  • Endothelial wellness
  • Nitric-oxide pathway support
  • Fibrinolytic balance research
  • Vascular-wellness routines under practitioner guidance
Practitioner Guidance Recommended

Designed for use inside a practitioner protocol — not a self-prescribed daily basic.

Nitric-Oxide Pathway

L-citrulline in Phase One paired with dietary nitrate from beetroot in Phase Two.

Fibrinolytic Balance Research

Nattokinase delivered in the phospholipid phase, kept separate from the cyclodextrin matrix.

Endothelial Antioxidants

Standardised pine bark OPCs in the phyto-active phase.

Complete ingredient explorer

Nothing hidden.

Final quantities are declared once formulation and regulatory review are complete.

IngredientRolePer servingEvidence
HPβCDAdvanced cyclodextrin researchTBCMechanistic
L-CitrullineNitric-oxide precursorTBCEmerging
NattokinaseFibrinolytic researchTBC (FU/serving)Emerging
Beetroot extract (standardised)Dietary nitrateTBCEmerging
Pine bark extract (standardised)Endothelial OPCsTBCEmerging
Sunflower phosphatidylcholineCholesterol-free liposomal carrierTBCEstablished
What makes AUREVIA CD//FLOW different

A practitioner-guidance formulation built around endothelial and circulation pathways.

Practitioner-first positioning

Not sold as a self-directed daily wellness item. Labelling and pack copy will direct consumers to qualified practitioner guidance.

Ingredient separation with intent

Nattokinase and lipid-soluble phyto-actives are stored away from the HPβCD-bearing aqueous phase to protect activity and inclusion behaviour.

Explicit medication cautions

Cautions for anticoagulant and antiplatelet medication are prominent, not buried.

Developed for
  • Adults working with a qualified practitioner
  • Consumers focused on endothelial and circulation-pathway support
  • Practitioners looking for a differentiated multi-pathway circulation format
  • Existing users of nitric-oxide precursors seeking a more considered format
Proposed use
Combine both chambers immediately before use. Use only according to the final approved product label. Final instructions will be established through formula validation, safety review, regulatory assessment, palatability testing, human tolerability evaluation and packaging validation.
Safety panel

Consult a qualified healthcare professional before use if you:

  • Are pregnant or breastfeeding
  • Take prescription medication
  • Have kidney or liver disease
  • Have diagnosed cardiovascular disease
  • Use lipid-lowering medication
  • Are receiving specialist medical care
  • Are preparing for surgery or another medical procedure
  • Have experienced sensitivity to cyclodextrins or formulation ingredients

Do not discontinue or replace prescribed treatment.

FAQ

Questions we get, answered honestly.

Can I take CD//FLOW if I use blood thinners?+

Not without specific clearance from your prescribing clinician. Nattokinase can affect fibrinolytic pathways relevant to anticoagulant and antiplatelet therapy.

Is CD//FLOW a treatment for cardiovascular disease?+

No. It is not a treatment for any disease and does not replace prescribed medication.

Why is it called a practitioner system?+

Because appropriate use, dose, timing and combination with other therapies is best assessed by a qualified practitioner.

Is the finished product clinically tested?+

Not yet. Ingredient-level research exists but is not equivalent to finished-product trials.