Immune Senotherapy
Vitality bioregulation
Human Ultracell®VIIMan
Immune Senotherapy
Vitality bioregulation
Human Ultracell VII – Man represents Biocell Ultravital’s most advanced regenerative therapy, scientifically formulated to meet the specific physiological needs of men 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 VII – Man 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 to address the specific challenges of male aging, it contributes to improved energy, physical performance, libido, cognitive clarity, and metabolic stability.
Whether used preventively or therapeutically, Human Ultracell VII – Man offers a proactive approach to sustaining vitality, resilience, and physiological strength over time.
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Below, we address common questions about Human Ultracell VII – Man to help you understand its regenerative and preventive potential.
Q1: What does Human Ultracell VII – Man support?
Human Ultracell VII – Man promotes hormonal balance, sexual function, muscle strength, energy, and immune performance. It helps reduce signs of cellular aging and supports long-term vitality in men.
Q2: Is this only for men with low testosterone or symptoms of aging?
No. Human Ultracell VII can be used as a preventive therapy starting as early as age 30. It is also beneficial for men experiencing hormonal shifts, fatigue, sexual decline, or chronic stress.
Q3: Can it improve libido and reproductive performance?
Yes. The formulation supports testosterone activity and neuroendocrine balance, improving libido, erectile function, and reproductive health by reinforcing hormonal signaling and cellular function.
Q4: Is it safe to combine with other therapies or medications?
Yes. Human Ultracell VII – Man can be used alongside other Biocell formulations or conventional treatments. We recommend consulting your physician to customize a full protocol.
Q5: What are opotherapeutic extracts and why are they used?
Opotherapeutic extracts are biologically active compounds sourced from porcine embryonic tissues. They contain regenerative molecules such as proteins, growth factors, enzymes, and cellular cofactors.
These embryonic tissues are highly potent, offering concentrated signals that promote cellular repair, hormonal stimulation, and tissue regeneration.
Because porcine-derived structures share over 90% biochemical compatibility with human cells, the body naturally integrates them without immune rejection. Human Ultracell VII protects these ingredients with enteric coating, allowing them to reach circulation intact for targeted delivery.
This therapeutic model has been used safely in regenerative medicine for over 70 years and continues to be refined with modern bioavailability technologies.
Human Ultracell VII: Man
Senotherapy
Cellular Renewal
Oral presentation.
Contains 7 different formulas per dosage.
7 tablets
differentiated in formulas, engraving and color of 750 mg
each
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Formula 1
Urolithin A, Thymosin Alpha -1, Thymosin Beta - 4, Fisetin, Espermidina, Casin, Astaxantina.
Opotherapeutic Extracts: Pancreas, Kidney, Placenta, Thymus, Embryo.
Peptide Extracts: Suprefort, Pielotax, Placenton, Thymalin, Embryon
Enzyme Complexes:Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP).
Other Assets: Adenosine Diphosphate (NAD) Dinucleotide, Phosphatidylserine, Propionyl Arginate, Riboflavin, Thiamine, Niacin, Hypericin, Vinpocetine, Pregnenolone, Coenzyme Q10, Coenzyme A, Stabilizers, and Excipients.
Formula 2
Urolithin A, Thymosin Alpha -1, Thymosin Beta - 4, Fisetin, Espermidina, Casin, Astaxantina.
Opotherapeutic Extracts: Adrenal Gland, Thyroid, Placenta, Thymus, Embryo.
Peptide Extracts: Glandokort, Placenton, Thymalin, Embryon.
Enzyme Complexes:Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP).
Other Assets: Adenosine Diphosphate (NAD) Dinucleotide, Phosphatidylserine, Propionyl Arginate, Riboflavin, Thiamine, Niacin, Hypericin, Vinpocetine, Pregnenolone, Coenzyme Q10, Coenzyme A, Stabilizers, and Excipients.
Formula 3
Opotherapeutic Extracts: Bone, Placenta, Thymus, Embryo.
Peptide Extracts: Umbilical cord, Embryo, Placenta, Thymus, Heart, Lung, Prostate.
Enzyme Complexes:Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP).
Other Assets: Adenosine Diphosphate (NAD) Dinucleotide, Phosphatidylserine, Propionyl Arginate, Riboflavin, Thiamine, Niacin, Hypericin, Vinpocetine, Pregnenolone, Coenzyme Q10, Coenzyme A, Stabilizers, and Excipients.
Formula 4
Opotherapeutic Extracts: Skin, Muscle, Placenta, Thymus, Embryo.
Peptide Extracts: Mesenogen, Placenton, Thymalin, Embryon.
Enzyme Complexes:Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP).
Other Assets: Adenosine Diphosphate (NAD) Dinucleotide, Phosphatidylserine, Propionyl Arginate, Riboflavin, Thiamine, Niacin, Hypericin, Vinpocetine, Pregnenolone, Coenzyme Q10, Coenzyme A, Stabilizers, and Excipients.
Formula 5
Opotherapeutic Extracts: Pituitary gland, Brain, Placenta, Thymus, Embryo.
Peptide Extracts: Pitulon, Pinealon, Placenton, Thymalin, Embryon.
Enzyme Complexes:Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP).
Other Assets: Adenosine Diphosphate (NAD) Dinucleotide, Phosphatidylserine, Propionyl Arginate, Riboflavin, Thiamine, Niacin, Hypericin, Vinpocetine, Pregnenolone, Coenzyme Q10, Coenzyme A, Stabilizers, and Excipients.
Formula 6
Opotherapeutic Extracts: Heart, Placenta, Thymus, Embryo.
Peptide Extracts: Chelohart, Placenton, Thymalin, Embryon.
Enzyme Complexes:Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP).
Other Assets: Adenosine Diphosphate (NAD) Dinucleotide, Phosphatidylserine, Propionyl Arginate, Riboflavin, Thiamine, Niacin, Hypericin, Vinpocetine, Pregnenolone, Coenzyme Q10, Coenzyme A, Stabilizers, and Excipients.
Formula 7
Opotherapeutic Extracts: Prostate, Testicles, Placenta, Thymus, Embryo.
Peptide Extracts: Libidon, Testoluten, Placenton, Thymalin, Embryon.
Enzyme Complexes:Superoxide Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP).
Other Assets: Adenosine Diphosphate (NAD) Dinucleotide, Phosphatidylserine, Propionyl Arginate, Riboflavin, Thiamine, Niacin, Hypericin, Vinpocetine, Pregnenolone, Coenzyme Q10, Coenzyme A, Stabilizers, and Excipients.
Indications:
- 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:
Human Ultracell Oral Protocol:
Indications for taking the product.
Posology 1 Preventive Therapy.
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:
Posology 2 Clinical Treatment.
Frequency and dose by age.
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:
Side effects:
Contraindication
In the recommended doses, no adverse reactions have been observed in any case.
Presentation and packaging:
Extraction and obtaining of biopeptides and cellular extracts
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.
Conservation:
Control of finished product:
Warning:
Mechanism of action
Human-Ultracell VII 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
How Does it Work?
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How the Formulas are Developed?
We strive to achieve perfection for each of our therapeutic categories, since they are formulated by carefully selecting each component after confirming its characteristics and clinical trials that positively compromise the efficacy in each formula, this is basically the science on which our products and therapies are based.
Biocell Ultravital products are formulated with ingredients that are 100% natural biological substances, with the highest quality standards, containing cellular extracts of animal origin and peptide hydrolysates extracted from plant extracts and glands of young animals in combination with antioxidants, enzymes and vitamins we managed to optimize the formulas and their therapeutic scope.
All raw material sources are carefully selected from organic plants and organs of pigs and sheep less than one year old and undergo a prion and decontaminated pharmaceutical standardization process that meets high biosecurity standards for reach specific concentrations of high purity and are processed under strict controls to guarantee the high quality and purity of their products.
No chemicals, other harmful or unwanted substances are used in the extraction. Modern technology ensures the recovery of assets in a biologically natural way, without changes. This is very important for the safety of each formula. None of the components in Biocell Ultravital formulas are genetically modified. (NON GMO)
Production and Extraction of Bio Peptides 4th Cellular Generation
After this, the hydrolyzate is fractionated by exclusion chromatography and semi-preparative liquid chromatography in reverse phase, selecting the fraction with the highest activity as a result of the first invitro tests, and finally the sequence of the peptides responsible for generating the activity is identified. The desired therapy is obtained by applying mass spectrometry and / or N-terminal sequencing. However, hydrolysates are complex mixtures and can contain up to hundreds of different molecules, therefore, locating bioactive peptides in these procedures is a biochemical work of constant expertise that results in a difficult task and requires a lot of time and dedication. The fractions usually still contain multiple compounds that require additional cycles of fractionation, concentration and evaluation of bioactivity to be able to identify the molecule responsible for the activity in the formulas of each product according to the therapeutic indication.
Consequently, the enzymatic hydrolysis used offers undoubted advantages, such as the absence of substrate degradation processes since the enzymes are selective for a type of bond, pH values between 5 to 10 and the temperatures between 40 to 60ºC, thus maintaining or improving the nutritional value of the protein. The specificity of the enzyme affects the size, quantity, and composition of free peptides and amino acids, as well as their amino acid sequence.
Safety in Therapies
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.
Research and Development
Working in the context of formulas based on opotherapeutic extracts or cells of xenogeneic origin, they aim to support the expansion of products for basically strengthening the immune system.
Cellular Renovation Therapy may contribute as reinforcement to the primary treatment to treat the various human diseases that are associated with failures of the immune system. In order to achieve this purpose the continuous efforts of a scientific committee structured by various institutions in the field biology headed by Prof. Dr. Ben L Pfizer is needed. These contributions guide new formulations that improve the components has been allocated to four fundamental guidelines with specific objectives corresponding to the 4th generation cellular products by Biocell Ultravital: Protection, Repair, Revitalization and Regeneration properties. These therapeutic lines are developed with a common research and development strategic plan for each product category.
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
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
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.
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