Human Ultracell VI – Woman represents Biocell Ultravital’s most advanced regenerative therapy, scientifically formulated to meet the specific physiological needs of women across different life stages.
This fourth-generation Cellular Renovation Therapy delivers potent regenerative signals through a synergistic combination of embryonic cellular extracts, biopeptides, antioxidant enzymes, and essential micronutrients, aimed at restoring functional balance and optimizing systemic vitality.
By activating the body’s natural repair mechanisms, Human Ultracell VI – Woman enhances mitochondrial performance, supports hormonal balance, strengthens immune defenses, and promotes the cellular renewal process — all essential pillars for preserving long-term health and well-being.
Designed for both preventive and therapeutic applications, it offers a proactive approach to cellular aging, helping women sustain energy, clarity, and resilience as they move through life’s transitions.
Key Benefits
• Hormonal Regulation: Supports endocrine equilibrium, assisting in the stabilization of hormonal fluctuations.
• Mitochondrial Enhancement: Increases cellular energy production, reducing fatigue and improving resilience by stimulating mitochondrial functions.
• Immune Modulation: Strengthens immune system performance and reduces inflammatory processes.
• Dermal and Tissue Health: Enhances skin elasticity and stimulates tissue regeneration.
• Skeletal Support: Contributes to bone density preservation and improves joint stability.
• Stress Resilience: Strengthens the body’s adaptive responses to physical and emotional stress.
Organic Aging and Cell
Renewal Therapies
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Below, we answer some of the most frequently asked questions about Human Ultracell VI to help you understand its unique regenerative approach.
Q1: Who is an ideal candidate for Human Ultracell VI – Woman?
Women seeking to enhance their cellular health, hormonal balance, immune resilience, and overall vitality — whether for preventive support or therapeutic needs.
Q2: How soon can results be expected?
While individual responses may vary, many users report improvements in energy, cognitive function, and overall well-being within the first few weeks of consistent use.
Q3: Can Human Ultracell VI – Woman be combined with other Biocell therapies or conventional treatments?
Yes. Human Ultracell VI is compatible with other Biocell formulations and can be integrated alongside conventional medical treatments. Consultation with a healthcare professional is recommended to personalize protocols.
Q4: Are there any known side effects?
Human Ultracell VI is formulated using biologically compatible, pharmaceutical-grade ingredients. No adverse effects have been reported when used as directed.
Q5: What are opotherapeutic extracts, and why are they critical to Human Ultracell VI’s effectiveness?
Opotherapeutic extracts are biologically active compounds sourced from ethically derived ovine embryonic tissues. These extracts contain vital proteins, growth factors, enzymes, and regenerative cofactors essential for cellular function and repair.
The embryonic origin ensures high regenerative potency, as embryonic tissues contain concentrated signals that drive cellular differentiation and healing.
Because ovine-derived bioactive molecules share over 90% biochemical similarity with human cellular structures, the body naturally recognizes and incorporates these regenerative factors without triggering immune response and rejection.
Following oral ingestion, Human Ultracell VI’s ingredients are protected by an enteric coating, allowing safe passage through the stomach into the intestine, where they are absorbed into circulation. This precise delivery method preserves their biological activity and promotes targeted tissue rejuvenation.
Historically, opotherapy has been a cornerstone of regenerative medicine for over 70 years, with a strong safety and efficacy profile. Modern advancements in purification and bioavailability have made these extracts even more effective for supporting systemic health and cellular vitality.
Human Ultracell VI: Woman Longevity
Activator. Oral presentation.
Contains 6 different formulas per dosage. 3
capsules differentiated in formulas, engraving and color of 750 mg each.
3 tablets differentiated in formulas, engraving and color of 750 mg
each
Dr. Patrick Human Ultracell
VI
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Regeneration, revitalization and cell renewal for human longevity, through
the reinforcement of the immune system.
Adjuvant in degenerative diseases of the immune system.
Premature aging.
Decreased mental and physical faculties, fatigue, physical asthenia.
Prevention of degenerative diseases.
General energy increase.
Revitalization of bodily functions.
Increased resistance to stress.
Improved performance and organic function that weakens with aging.
Remarkable improvement in physical performance.
Improved blood pressure.
Recovery of concentration and memory capacity.
Improved quality of sleep.
Prevention of osteoporosis.
Stimulation and control of libido in men and women.
Strengthening of the venous system, acceleration of wound recovery.
Stimulation of endogenous production of growth hormone that maintains muscle
mass.
Prevention of senescence keeping the patient as a young adult.
Administration:
Orally, consume before taking food to improve absorption, preferably with water
in the morning.
Dosage:
Corresponds to 4500 mg for each daily dose consisting of the contents of 1 vial
containing 6 pills (capsules and/or tablets) of 750 mg each. Each pill is
specially formulated for prolonged release to withstand digestive enzymes
facilitating absorption in the small intestine. Daily doses are provided in the
contents of individual vials intended to be taken daily. We recommend the
contents of each vial be taken once opened within that day. The packaging is
comprised of 3 cycles containing 5 daily doses each (15 vials total). Treatment
should be implemented in the following nature Cycle 1 for 5 days taking contents
of 1 vial daily (six pills). Cycle 1 should be followed by Cycle 2 for 5 days
consuming the contents of 1 vial daily. Cycle 2 should be followed by Cycle 3
for 5 days consuming contents of one vial daily. This 15-day regiment should be
repeated for another 15 days in the same manner to complete a 30 day monthly
recommended treatment. This dosing should be completed without intervals or
interruption. Follow up dosing should be implemented according to patient’s age
and doctor recommendation.
Human Ultracell VI Oral Protocol:
Depending on the condition and age, the dosage orientation varies to optimize
the effectiveness of the treatment.
Indications for taking the product.
Posology 1 Preventive Therapy.
As preventive therapy in asymptomatic patients to prevent degenerative diseases
and slow down aging.
Frequency and dose by age.
From 30 to 39 years 30 doses and repeat every 6 months. *
From 40 to 49 years 30 doses and repeat every 4 months. *
From 50 to 59 years 30 doses and repeat every 3 months. *
After 60 years, 30 doses and repeat every 2 months. *
* Each dose corresponds to one dose per day.
* Restart annually for equal periods according to age.
IMPORTANT:
Do not interrupt the recommended doses of treatment, its therapeutic effect is
of continuous action, its effectiveness will depend on the completion of the
treatment.
Posology 2 Clinical treatment.
As Adjuvant Therapy for symptomatic
patients suffering from a disorder or disease, or people with a marked family
genetic inheritance to contract diseases.
Frequency and dose by age.
From 30 to 39 years 45 doses every 6 months.
*
From 40 to 49 years 45 doses every 4 months. *
From 50 to 59 years 45 doses every 3 months. *
After 61 years 45 doses every 2 months. *
* Each dose corresponds to one dose per day.
* Restart dose cycles for equal periods annually.
Chronic diseases it is recommended to consult a doctor for the corresponding
indication.
IMPORTANT:
Do not interrupt the recommended doses, its therapeutic effect is of continuous
action, its effectiveness will depend on the continuity of the treatment.
Side effects:
Due to its peptide and opotherapeutic content in its formula, it could in some
cases cause a slight headache, which disappears after a few minutes, nausea is
very occasional and disappears in a few hours.
Extraction and obtaining of biopeptides and cellular extracts
It should
be noted that the formulas contain biological components of animal origin in
combination with other compounds that enhance the therapeutic action and are
extracted especially in the embryonic stage and processed during the second
month of gestation, these components that are part of the formulas of some of
Our products are obtained after a long biochemical process and are certified
free of prions, pyrogens, bacteria, nano-bacteria, fungi, viruses and after many
controls, the risks of an immune reaction in Humans are 100% eliminated.
Many years of clinical experience has shown that pigs and sheep are the best
donors, because they are strong and immunologically resistant. Proof of this is
that even in the 21st century, most heart valve transplants for humans are
derived from pigs, in addition to insulin and many derived products for
therapeutic purposes, come from these. These methods are continuously monitored
to determine that they meet the strictest standards required by biosafety for
therapeutic purposes. All the components and other active ingredients of the
formulas are manufactured in the USA by BIOCELL
ULTRAVITAL USA under Swiss license from Biocell
Ultravital.
Contraindication.
It can be safely combined with other medications.
In the recommended doses, no adverse reactions have been observed in any case.
Presentation and packaging:
Contains 45 enteric-coated tablets and 45
enteric-coated capsules with engraving and different colors that are packaged in
15 sterile vials with stoppers and security seal with the printed name of the
brand on tear-off to preserve quality of each of its different formulas and
presentations.
Conservation:
Keep in a dry and cool place at room temperature between 5
° C and 40 ° C. Do not use after the expiration date, nor when the present vial
has broken the safety cap, nor when the outer packaging is open or forced.
Control of finished product:
Two (2) independent laboratories perform various tests and mycotic controls,
biological, bacteriological type 5 analyzes, multicenter immunocellular tests,
Anti brucellosis, Virological controls, multiple anti-prion tests, Bacteriosis,
Cyclospores, Mycobacteria, Salmonellosis in accordance with the subject of
biology for therapeutic purposes for human consumption according to current EC
regulations
Warning:
Biocell Ultravital guarantees the purity and quality of its
products and is not responsible for damage to third parties that may cause
malpractice.
Mechanism of action
The Human Ultracell VI formula
contains cellular and phytochemical biological compounds, which are administered
to the patient orally or intramuscularly, and once in the body are transported
to the bloodstream reaching the blood capillaries and from there to the
extracellular matrix. The extracellular matrix is a network of molecules,
proteins and carbohydrates that are arranged in the intercellular space and that
are synthesized and secreted by the cells themselves. From the extracellular
matrix the components of the formula pass into the cells, through the cellular
means available for it, mainly endocytosis.
Human-Ultracell VI contains a large number of cellular
components, embryonic growth factors, nucleotides and cytokines, which require
massive incorporation into the cell. In this massive incorporation,
extracellular molecules can enter the vesicle nonspecifically, in solution, or
specifically bound to membrane receptors, termed endocytosis and pinocytosis.
Endocytosis consists of a transport medium according to which the cell forms a
depression in its membrane, which engulfs the elements to be incorporated,
forming a vacuole that then closes around these elements and transports them to
assimilation and digestion bags called Lysosomes, where they are catabolized and
assimilated.
Pinocytosis is a type of nonspecific endocytosis of dissolved molecules. Some of
the contents of any vesicle that forms on the plasma membrane will have
dissolved molecules that have seeped into the vesicle in a non-specific manner.
To a greater or lesser extent, all endocytosis routes carry out pinocytosis.
Cycles of the Mechanism of Action
The cell renewal process
occurs continuously and its efficiency depends on the physiological state or
physiological age of the patient, in other words on their degree of
deterioration. Although we cannot speak of defined stages of therapy action, we
can use the concept of cycles to define the sequence of its renewal processes.
CYCLE 1
CELL REVITALIZATION: The high content of coenzymes NAD
(Nicotinamide Adenine Dinucleotide) of the formula, essential for the efficient
production of energy of the cell, in the phase of Oxidative Phosphorylation,
together with the inducers of proliferation of mitochondria of the formula,
almost immediately contribute to increasing the production of cellular energy,
which allows cells to develop a process of AUTOPHAGY, cell cleaning, to get rid
of denatured proteins and other useless biological material, accumulated in
their cytoplasm as a result of poor functioning cell functions over time. Said
biological material is digested in lysosomes, or vesicles of digestion by
hydrolase enzymes, to be reused in the production of new proteins for the body.
Cells freed from the overwhelming burden of biological waste, and with increased
energy production, undergo a great revitalization. It is important to note that
AUTOPHAGY takes on special significance in the case of cells that do not divide,
such as neuronal and cardiac cells, and those that divide little, reducing the
risk of accumulation of harmful proteins that hinder their functions. It is
worth mentioning that Alzheimer’s disease is associated with the accumulation of
amyloid proteins in neurons. It has recently been discovered that the coenzymes
NAD are not only essential for the efficient production of cellular energy,
adenosine triphosphate (ATP), but also that they are key for efficient
intracellular communication in the chronological execution of their functions,
hence a decrease in its amount in cells, contributes to aging.
CYCLE 2
CELL RENEWAL: With the progressive recovery of the energy
production capacity induced by the formula and by the effects of the growth
factor stimulating cytokines in the formula, a process of normalization of
cellular functions begins, particularly its machinery for the production of
membrane proteins and lipids. In this cycle, the controls in the transcription
of DNA into messenger RNA and translation into proteins are also reinforced, to
avoid errors in the amino acid sequence of said proteins. In addition, the
semi-conservative replication mechanisms of DNA are reinforced, prior to mitosis
at the cellular interface and the cellular capacity to correct copying errors.
In addition, cells improve their protection mechanisms against mutations,
reinforcing their capacity for apoptosis of mutated cells.
CYCLE 3
ORGANIC RECOVERY: The normalization of cellular functions leads to a
greater production of proteins, which translates into an increase in muscle
mass, an increase in collagen in the skin, joints, connective tissue,
improvement of liver, kidney, and lung function, cardiovascular, in addition to
cognitive functions, memory, ability to concentrate, etc. and stimulates the
immune system. The synergistic action of the amino acids and catalyst peptides
of Human Ultracell induces and stimulates the pituitary gland to release a
greater proportion of human growth hormone (whose production decreases
appreciably with age), which acts directly on all tissues of the body, causing
the activation of a younger metabolism, characterized by an increase in protein
synthesis in almost all cells of the body, increased mobilization of fatty acids
from adipose tissue, increased amount of free fatty acids in the blood and
preferential use of fatty acids as an energy source instead of glucose. This
cycle almost always begins in week 3 or 4 and reaches its peak within 6 months.
Safety in Therapies
Safety control is a very important factor, especially when it comes to high quality health products, which is why at Biocell Ultravital in France, which is the main headquarters where all the research and development of the formulas take place, we have monitoring and follow-up mechanisms for each product, this to prevent any error in the next production, that is why we are continuously implementing software for the detection of technical failures of the human team in charge of production. This translates into maximum safety controls that guarantee the complete quality of the production, eliminating 100% possible adverse reactions due to the indication of some of our products that does not correspond to a contraindication already described.
This discipline has become responsible for quality control in the formulation and manufacturing phases thanks to the detection, evaluation, knowledge and analysis for the prevention of adverse reactions and other possible problems related to the products, covering a wide spectrum of continuous analysis so that they do not cause any harm to the patient. We actively participate in decision-making when manufacturing to prevent possible complications in any of the production stages. Thanks to the standardization and development of specific protocols established for each production and subjected to continuous analysis adhering to very specific guidelines we are able to prevent these unwanted complications.
Biocell Ultravital France
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Biocell Ultravital USA
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Manufacturing Plants and Procedures
In Europe, research, production and development is carried out at Biocell Ultravital, France, and we share part of the manufacturing in two other associated plants, mainly for the production of some raw materials, between Germany and the Netherlands.
We also manufacture our products in the USA, BIOCELL ULTRAVITAL USA Laboratories, where we have a modern production factory especially for manufacturing formulas and products for oral presentation.
Since our products formulas require components be extracted from a biological source, in all manufacturing plants we have ensured that they are manufactured in production rooms that have state-of-the-art equipment controlled by software that manages the procedures monitoring each phase of the process. Development with the latest air conditioning, quality and safety systems, to ensure that the final product does not lose its therapeutic potency, for this reason the active ingredients of each formula and the preparation in the initial phase are conditioned in isolated clean rooms and by specialized professionals trained to measure and control the production process from the moment this first manufacturing phase begins and continuing these quality controls through each phase of production until the final product is approved.
Products that Improve Cellular Renovation
Currently there is a growing interest in cell therapy extracted from the patient’s own stem cells, unlike our products, Cellular renovation therapies (CRT) provide sustained results without complications and represent a great economic saving in comparison. The products in the Biocell Ultravital line of Cell Renewal Therapies are divided into 5 main groups that include: Regeneration, Revitalization, Detoxification, De-inflammatory and Hormonal.
CRT have worked with great success in recent years as a preventive treatment, without discarding its effective action as a primary therapeutic. The treatment benefits are notorious for their adjuvant action in allopathic medicine. CRT, through their formulas, exclusively allow us to transform diseased or aging organs into healthy organs with a highly functional capacity. Their components activate a series of stimuli that cells need for a normal cycle of continuous renewal, and they can be incorporated into the body through injections or orally. These various components are assimilated by the body through endocytosis and a good part is introduced into the cells. This is produced by the emission of pseudopods until they completely encompass it to form a vacuole, which then fuses with the lysosomes to degrade the phagocytosed substance, which is known by the name of phagosome. This method is characterized by being the mode of nutrition used by cells through ingestion of foreign matter. In addition, it is one of the greater means of transport that they use to defend themselves against some cells of multicellular organisms.
From this mechanism and many other stimulating biochemical changes, nutrition begins for an effective CELLULAR RENOVATION (CRT). brings a fresh genetic information contained in DNA and RNA, stimulating secretion inducing old or sick cells and reprogramming to operate properly, providing the recipient bodies, a large number of biochemical and enzyme substrates containing information needed to revitalize an organ, or a gland. CRT contains various compounds that are primarily responsible for properly nourishing cells, but, moreover, each of the formulas in a CRT contains cells and embryonal tissues that increase positive changes in cell cycle complementing in part dysfunctional lapses. This is how the different components are first incorporated as essential nutrients and as well, how the embryonic tissues reach the organ with low vitality and that need to be dynamized. This process is called CELLULAR RENOVATION and its benefits are perceived after several weeks, as it passes slowly from the cell to the tissue, from the tissue to the organ and from the organ to the system. Some specialists feel that the most important result of using CRT is the revitalization of the body’s immune defense mechanisms. When damage occurs to the cells that make up the different tissues and organs involved in the immune system, either through aging or environmental poisoning, the body becomes defenseless from both external invasion and internal degeneration. The damage caused to the organs of the immune system can be reversed by stimulating the body’s defense mechanisms to boost the health of the weakened organ.
Security System to Prevent Falsification
Biocell Ultravital has developed for the 4th generation a sophisticated security system for its products to prevent the repetition of copies and / or counterfeiting of our products. Moving forward, we will invest a great technological effort in each package to ensure that you will have an original product in your hand.
This security system is applied to new packaging that have a QR Scan code applied to a double security system, a first physical stage in the packaging that will reveal through a security tab if the product has been violated and a second with an implantation of sophisticated software that will allow you to check if the product you purchased is original through our website, or by downloading the new BIOCELL APP for Android and IOS for free.
The falsification of ethical and health products is a problem that is becoming increasingly important, and all the different therapeutic areas may be affected.
These counterfeits seek to pass for authentic products, copying the packaging material, the commercial image, the logo, the information brochures, as well as the shape and colors of the original product.
In addition, they use the same lot number, expiration date and other identifying elements of the authentic product. However, they are manufactured and placed on the market without the authorization of any health authority. These original and generic medicines, as well as vitamins are also falsified and even more so those products that enjoy prestige are the most vulnerable and these falsifications may contain active ingredients in incorrect doses or lower doses than those authorized, or the absence of active ingredients and even include some toxic elements. Many may even be manufactured under dangerous conditions that are not controlled. Thus, they can pose a significant risk to health and are sometimes especially difficult to identify.
In short, they look identical to the original product, but contain “uncontrolled” components that are life threatening.
he trade in counterfeit medicines is controlled by international criminal networks, and no region is exempt. Those countries with less controlled drug distribution systems are more vulnerable to this type of practice; However, the most developed countries are not spared from this evil, especially when patients purchase drugs on the internet or unauthorized websites. Unfortunately, in the past we have been victims of these unethical organizations and have had to report these facts to the authorities since many people especially in Asian countries, as well as Mexico and others in Central and South America are victims of misleading offers of therapies, even by unethical doctors who offer the products at prices lower than the real cost. However, in the end they spend more money due to the need to seek immediate clinical help as demonstrated on several occasions reported by us through our attorneys around the world from patients who were treated clinically for administering fake products.
Human Ultracell VI – Woman is grounded in decades of clinical research across regenerative medicine, cellular therapy, organotherapy, and complementary preventive medicine.
Its formulation reflects the understanding that cellular degeneration — whether due to aging, stress, or chronic disease — can be delayed or partially reversed through targeted biological support.
Unlike synthetic interventions, Human Ultracell VI harnesses naturally compatible compounds that interact with the body’s intrinsic repair systems, strengthening immune defenses, hormonal pathways, and metabolic functions from the inside out.
The combination of opotherapeutic extracts, antioxidant enzymes, and cellular cofactors allows for a holistic yet scientifically sophisticated approach to restoring balance at the cellular and systemic levels.
Biocell Ultravital remains committed to advancing research into cellular renovation, continuously refining protocols based on the latest scientific findings to optimize patient outcomes ethically and effectively.
Scientific bibliographies.
In 1980 Jean Dausset was awarded the Nobel Prize
in Medicine for demonstrating that genetically determined cell surface
structures regulate immunological reactions, inspiring in this scientific
contribution Wagman decided to incorporate
immunological extracts into the formulas of all first-generation Biocell
Ultravital products in order to strengthen the immune system.
In 1999, Günter Blobel won the Nobel Prize in Medicine for
his work in the 1970s, discovering that proteins have intrinsic signals that
govern their transport and location in the cell.
In 2001 Paul Maxime Nurse was the winner of the Nobel Prize
in Physiology or Medicine for his discoveries of key regulators of the cell
cycle.
In 2007 Martin John Evans was awarded the Nobel Prize in
Medicine for his work on stem cells and genetic manipulation in animal
models.
In 2016 Yoshinori Ōsumi received the Nobel Prize in
Medicine” for his discoveries on the mechanisms of autophagy for survival of
mitochondrial energy in cells.
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