Nutraceutical

Senactiv® – Botanical Ingredient Details | Mediocon Inc.

Nutraceutical GMP Certified Aurangabad, Maharashtra, India
Senactiv® – Botanical Ingredient Details | Mediocon Inc. — Mediocon Inc
Senactiv® – Botanical Ingredient Details | Mediocon Inc.

Product Overview

Category: Nutraceutical

Senactiv® – Premium Botanical Extract Ingredient

Product Overview

Senactiv® is a proprietary botanical ingredient developed by NuLiv Science, combining extracts from Panax notoginseng root and Rosa roxburghii fruit. It is used as an ingredient in selected nutraceutical and dietary supplement formulations.

The ingredient is designed for formulators interested in botanical extracts with defined analytical markers. Its quality profile and suitability for a particular application should be evaluated using the current manufacturer specification, batch Certificate of Analysis (CoA), and applicable regulatory documentation.

Composition and Botanical Sources

Panax notoginseng root extract: Panax notoginseng is a botanical species traditionally used in East Asian herbal practices. Its root contains naturally occurring saponins, including ginsenosides. Senactiv® product documentation identifies ginsenoside Rg1 as one of its analytical markers.

Rosa roxburghii fruit extract: Rosa roxburghii is a fruit-bearing plant native to parts of China. Its fruit contains naturally occurring vitamin C and polyphenolic compounds. The specific compounds and their concentrations in Senactiv® should be confirmed using the current product specification.

These extracts are processed and standardized as a proprietary ingredient. Botanical identity, extraction methods, component ratios, carriers, and marker levels should not be inferred from the plant names alone.

Technical Standardization and Quality

Supplier documentation dated August 2025 identifies ginsenoside Rg1, vitamin C, and total polyphenols among the analytical markers for Senactiv®. The same documentation describes a powder ingredient processed using water and ethanol extraction.

The published specification sheet also includes information on appearance, particle size, loss on drying, ash, bulk density, solubility, heavy metals, pesticide residues, residual solvents, and microbiological controls. These values are grade-specific and should be confirmed against the latest approved TDS and batch CoA before being used for purchasing or quality decisions.

Potential Formulation Applications

Senactiv® is marketed for use in nutraceutical formulations, including products developed around exercise performance, physical recovery, and cellular health. The relevance of published research depends on the studied formulation, dose, population, and outcome. Ingredient research does not guarantee the same effects in every finished product.

Senactiv® should not be represented as a treatment for disease, a proven anti-aging therapy, or a substitute for medical care. Health-related marketing statements should be supported by appropriate evidence and comply with the regulations applicable to the intended market.

Quality Documentation and Sourcing

Before selecting Senactiv® for a formulation, request the current Technical Data Sheet (TDS), batch Certificate of Analysis (CoA), Safety Data Sheet (SDS), botanical identity confirmation, analytical methods, contaminant results, shelf-life information, and applicable certification or regulatory documents.

Mediocon Inc. can be contacted to confirm whether this specific branded ingredient is available, along with its grade, packaging, quantity, documentation, and commercial terms.

Product Specifications

Product NameSenactiv® – Botanical Ingredient Details | Mediocon Inc.
CategoryNutraceutical
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Analytical Specifications

ParameterSpecification
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Sourcing, Regulatory & Export Information

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Senactiv® – Botanical Ingredient Details | Mediocon Inc. and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Senactiv® – Botanical Ingredient Details | Mediocon Inc. is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.

Export Markets

  • USA — FDA-registered facility; DMF support available for ANDA/NDA filings
  • Europe — EMA-compliant documentation; CEP/EDMF support on request
  • Africa & Middle East — WHO-GMP certified; competitive pricing for emerging markets
  • Southeast Asia — established logistics network; temperature-controlled shipments
  • India domestic — schedule H/X compliance; all state licensing documentation provided

Quality & Compliance

  • ISO 9001:2015 certified quality management system
  • GMP-certified manufacturing facility, Aurangabad, Maharashtra
  • Full batch traceability from raw material to finished API
  • Dedicated QA team for customer audits and regulatory queries

Frequently Asked Questions — Senactiv® – Botanical Ingredient Details | Mediocon Inc.

1. What is Senactiv®?
Senactiv® is a proprietary botanical ingredient developed by NuLiv Science, combining Panax notoginseng root extract and Rosa roxburghii fruit extract.
2. What are the botanical ingredients in Senactiv®?
The current supplier specification identifies Panax notoginseng root and Rosa roxburghii fruit. Confirm the botanical names against the current product documents.
3. What is Senactiv® used for?
It is incorporated into selected nutraceutical and dietary supplement formulations, including products marketed around exercise performance and recovery.
4. What is ginsenoside Rg1?
Ginsenoside Rg1 is a naturally occurring saponin associated with Panax notoginseng. Supplier documentation identifies it as an analytical marker for Senactiv®.
5. Does Senactiv® contain vitamin C?
The supplier specification lists vitamin C as a marker with a reference minimum of 0.6%. Confirm the current specification and batch CoA.
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