Medicinal plants in functional beverage formulation can provide functional beverages with polyphenols, flavonoids, anthocyanins, terpenoids, alkaloids and volatile aromatic compounds. For manufacturers, successful formulation depends not only on selecting a botanical, but on controlling its identity, extract specification, target dose, stability, sensory impact and regulatory suitability throughout processing and shelf life
Dr Ananya Sharma, PhD (Phytochemistry & Food Technology)
Specialization: Functional Beverages, Botanical Extracts & Formulation Science
Medicinal plants in functional beverage formulation can provide functional beverages with polyphenols, flavonoids, anthocyanins, terpenoids, alkaloids and volatile aromatic compounds. For manufacturers, successful formulation depends not only on selecting a botanical, but on controlling its identity, extract specification, target dose, stability, sensory impact and regulatory suitability throughout processing and shelf life
Functional beverages increasingly incorporate botanicals with defined phytochemical profiles, creating opportunities for medicinal plants in functional beverage formulation. For product development, botanical selection involves more than choosing an ingredient associated with a particular benefit. In herbal product formulation, developers need to consider botanical identity, plant part, extraction method, marker compounds, dose, matrix compatibility, stability, sensory profile, safety and regulatory requirements.
These factors are important for the B2B product developer in terms of the ingredient specifications, processing conditions and the performance of the finished beverage. An extract which works well in a raw material test may act differently in its diluted, heated, pH-modified, flavoured, oxygen-exposed and stored form. [1]
With increasing demand for beverages positioned around gut health, immunity, cognition and stress-related benefits, functional beverage development is increasingly incorporating plant-based nutraceutical beverages with defined bioactive profiles. A 2026 review in Food Science & Nutrition highlights bioactive preservation, sensory quality, dosage, safety and regulatory considerations as key priorities. For manufacturers, this means botanical selection must be linked to how the ingredient performs in the finished beverage, from processing through shelf life. [2]
For B2B functional product development, botanical selection should consider:
Food Research Lab evaluates bioactive compounds, marker profiles, extraction characteristics and ingredient compatibility so manufacturers can select botanicals on a clear technical basis for functional beverage development.
Different classes of plant secondary metabolites behave differently in beverage matrices, so understanding bioactive compounds in functional beverages is important when developing herbal ingredients for functional drinks. For B2B formulators, the key question is not simply which compounds are present, but whether their concentration, stability, sensory impact and delivered dose can be controlled throughout processing and storage. [3]
Polyphenols include flavonoids, including anthocyanins, as well as phenolic acids. Green tea catechins, hibiscus anthocyanins and turmeric curcuminoids are well-studied examples of antioxidant plant compounds, yet they show different stability depending on the botanical origin, processing conditions and the beverage matrix. The 2026 Food Science & Nutrition review cites studies reporting significant degradation of hibiscus anthocyanins and green tea catechins at temperatures above 70°C. Therefore, thermal exposure should be evaluated under the actual beverage process rather than treated as a universal temperature cutoff. [2]
Essential oils are complex mixtures of volatile aromatic compounds, including terpenes and oxygenated terpenoids, that contribute to aroma and flavour. The volatility, oxidation tendency, and low water solubility of essential oils create problems related to their formula development and shelf life. [1]
A 2025 study of black tea supplemented with clove, mint, rose, and green tea identified changes in key aroma-active compounds and the beverage’s sensory profile, illustrating how aromatic plant ingredients can influence both aroma and overall beverage characteristics. [4]
For aromatic plant extracts for beverages, formulation should therefore consider volatile-compound profile, extraction method, concentration, matrix compatibility, dispersion and stability to maintain the intended sensory profile and any evidence-supported functional positioning.
Alkaloids, saponins, phytosterols and other specialized plant components can possess specific activity depending on their type and dose. Controlled dosing is especially important for caffeine-containing botanicals because concentration directly affects delivered dose and sensory characteristics. Herbal extract standardization using appropriate marker compounds can support batch consistency, specification control and formulation reproducibility. [3]
Table 1. Bioactive Compounds and Formulation Considerations
|
Compound class |
Representative plants |
Key bioactives |
Main formulation risk |
|
Polyphenols / Flavonoids |
Green tea, hibiscus, turmeric |
Catechins, anthocyanins, curcuminoids |
Heat degradation, astringency, bitterness |
|
Essential oils / Aromatics |
Peppermint, rosemary, clove, citrus |
Terpenoids, monoterpenes and other volatile constituents |
Volatility, oxidation, poor water solubility |
|
Alkaloids |
Guarana, green coffee |
Caffeine and related alkaloids |
Dose control, bitterness |
|
Steroidal lactones / Triterpenoid saponins |
Ashwagandha, ginseng |
Withanolides, ginsenosides |
Standardisation, dose control, matrix compatibility and claim substantiation |

FIGURE 1 Bioactive-to-Beverage Formulation Pathway.
A stepwise framework linking botanical selection, extract specification, target dose, formulation, processing, sensory and stability testing, pilot-scale validation, regulatory review, and commercialisation.
A major formulation challenge with medicinal plants in functional beverage formulation is maintaining the intended bioactive profile and delivered dose during processing and storage. Four factors require particular attention: stability, bioavailability, encapsulation and sensory performance:
Define the target marker compound and dose, then evaluate the finished beverage for solubility, pH compatibility, colour, aroma, oxidation, processing stability and sensory acceptance. A formulation that performs well at bench scale should also be reassessed during pilot and scale-up trials as part of functional beverage development, because changes in mixing energy, heating profile, oxygen exposure, hold time and packaging can affect bioactive retention and sensory performance.

FIGURE 2 Factors Influencing Bioactive Retention During Beverage Shelf Life.
Conceptual illustration based on published encapsulation and beverage-delivery literature; not a quantitative dataset.
Food Research Lab supports extract selection, encapsulation strategy, stability assessment and sensory validation for aromatic plant extracts for beverages and other botanicals, helping manufacturers evaluate whether target compounds remain within specification through processing and shelf life.
Regulatory status is based on the botanical, type of product, composition, dosage, use and target market. As a result, functional beverage ingredient sourcing needs to consider regulatory and botanical ingredient safety screening right from the outset. Companies must determine the product category, ingredient status, composition requirements and claim information before making the formulation and artwork decisions.
For B2B functional product development, early regulatory review helps align functional beverage ingredient sourcing, formulation specifications, evidence and claims before scale-up.
Table 2. B2B Regulatory Checkpoints for Botanical Beverages
|
Market |
Regulatory framework |
Key requirement |
B2B action |
|
EU |
Novel Food Regulation (EU) 2015/2283; Nutrition and Health Claims Regulation (EC) 1924/2006 |
Establish Novel Food status and assess applicable claims |
Verify food-use history, authorisation status and claim pathway before launch |
|
USA |
FDA conventional food and dietary supplement framework |
Determine product category and applicable claim type |
Establish ingredient, labelling and substantiation requirements before finalising claims |
|
India |
Applicable FSSAI food/nutraceutical framework |
Confirm product category, ingredient eligibility, composition and labelling requirements |
Verify regulatory status and permitted claims before scale-up |
|
UK (GB) |
GB Novel Food and claims framework |
Establish Novel Food status and applicable claim requirements |
Verify status/authorisation and claims pathway before launch |
|
All markets |
Market-specific food safety and claims requirements |
Confirm identity, dose, contaminants, evidence and intended use |
Align sourcing, specifications, stability, testing and claims before commercialisation |
Brief: A 2025 Life study (with a 2026 correction) evaluated Moringa oleifera leaf infusion as a functional beverage using phytochemical analysis and a high-fat-diet murine model.
Approach: Researchers measured polyphenol content and antioxidant activity, then assessed the metabolic effects of prophylactic infusion in high-fat-diet-fed mice.
B2B takeaway: The study illustrates how botanical preparation can be paired with chemical characterisation and preclinical biological evaluation. However, the findings are from a murine model and should not be interpreted as evidence of human clinical efficacy. Commercial plant-based nutraceutical beverages still require product-specific assessment of dose, safety, stability, sensory performance and claim substantiation.
Medicinal plants in functional beverage formulation can support product differentiation when bioactive stability, sensory quality, safety and regulatory compliance are controlled. Nutraceutical beverage development should be validated at the level of the finished beverage and not only in the raw extract form. Food Research Lab supports evidence-led herbal product formulation from botanical selection and extraction through formulation, analytical testing, sensory evaluation, stability assessment, regulatory review, pilot trials and scale-up.
Some examples include polyphenols such as flavonoids, anthocyanins, and phenolic acids, as well as volatile compounds of essential oils, terpenoids, alkaloids, and other plant secondary metabolites. Their concentrations and stability are a function of many factors, including botanical species, plant material used, and extraction process.
Some of these include bioactive degradation, insolubility, variability in bioavailability, bitterness, astringency, volatile-component loss and batch-to-batch variability. Herbal extract standardization, suitable delivery systems and formulation strategies can address some of these challenges, but performance should be verified in the final product.
Encapsulation can improve the bioavailability of some compounds, depending on the bioactive, delivery system and beverage matrix. Human studies have reported improved bioavailability for compounds such as hesperidin, fisetin and curcumin, while findings for some anthocyanin-rich preparations remain inconsistent. Improved stability does not necessarily indicate improved human bioavailability or clinical efficacy.
No. Factors that determine appropriateness include botanical identity, part of the plant used, extraction technique, required dose of the compound, specification of the ingredients, safety, contamination, solubility, sensory characteristics, processing stability, shelf life and target-market regulatory requirements.
Manufacturers should verify botanical identity, ingredient specifications, marker compounds, contaminants, microbiological quality and relevant lot-specific COA documentation. The finished beverage should then be assessed for formulation compatibility, processing stability, sensory acceptance and shelf life, followed by regulatory and claim review before commercial launch.
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