Carotenoids Market by Source (Natural, Synthetic), Form (Emulsion, Liquid, Oil Suspension), Type, Application - Global Forecast 2025-2032
Description
The Carotenoids Market was valued at USD 2.50 billion in 2024 and is projected to grow to USD 2.65 billion in 2025, with a CAGR of 6.65%, reaching USD 4.19 billion by 2032.
Positioning carotenoids at the intersection of science, consumer demand, and industrial innovation to explain contemporary commercial and functional relevance
Carotenoids are a diverse class of pigmented compounds with critical roles across nutrition, health, and industrial applications, and they have attracted sustained interdisciplinary interest from scientists, formulators, and procurement professionals. In recent years, advances in extraction technologies, fermentation platforms, and formulation science have reshaped how carotenoids are produced and integrated into end-use applications, prompting a shift in value chains and partnerships. This introduction sets the stage by outlining essential biochemical characteristics, principal commercial types, and the functional attributes that drive application-specific demand.
Building on biochemical foundations, the narrative then considers how consumer health trends, regulatory evolutions, and manufacturing innovations converge to expand both traditional and emerging uses. Dietary supplement manufacturers emphasize bioavailability and label transparency, cosmetic brands foreground antioxidant and color stability properties, and feed formulators prioritize performance and cost-effectiveness. As a result, stakeholders across research and commercial ecosystems are rethinking sourcing strategies, due diligence frameworks, and go-to-market approaches to capture differentiated value while managing regulatory and supply-chain complexity.
How technological advances, sustainability focus, and regulatory evolution are reshaping production, formulation, and sourcing strategies across the carotenoids ecosystem
The landscape for carotenoids is undergoing transformative shifts driven by technological maturation, shifting consumer expectations, and supply-chain resilience priorities. Innovations in microalgae cultivation, precision microbial fermentation, and greener extraction chemistries are elevating the competitiveness of natural production pathways, enabling higher yields, improved purity profiles, and reduced environmental footprints. At the same time, formulation science has progressed, enabling novel delivery formats that enhance stability and bioavailability, thereby opening new application windows in functional foods and personalized nutrition.
Concurrently, consumer preferences for clean-label and sustainably sourced ingredients are prompting brand owners to demand greater traceability and provenance documentation. This dynamic is catalyzing upstream investments in traceable supply chains and third-party verification schemes. Regulatory frameworks are also evolving, tightening requirements around claims, labeling, and permissible use in certain jurisdictions. As a result, firms that couple technological capability with rigorous compliance and transparent communication are gaining differentiation, while those that rely on commoditized supply without demonstrable stewardship face reputational and operational risks.
Examining the operational and strategic ramifications of evolving United States tariffs on supply chains, sourcing decisions, and regional production incentives in 2025
Recent tariff adjustments in major markets have introduced new layers of operational complexity for manufacturers, ingredient traders, and end-product companies that depend on cross-border flows of raw materials and intermediates. Tariff changes influence sourcing strategies, push firms to reassess supplier diversification, and can alter landed costs in ways that affect formulation choices and long-term contractual arrangements. In response, many organizations have prioritized nearshoring, expanded local production capabilities, or renegotiated supplier agreements to preserve margin and continuity of supply.
Beyond immediate commercial effects, tariff-driven dynamics can accelerate structural shifts in regional value chains. For instance, increased duties on certain imported ingredients can incentivize investment in domestic fermentation or cultivation capacity, with consequential impacts on logistics, capital allocation, and workforce development. Meanwhile, trading firms and distributors have adapted by broadening their supplier base, investing in compliance and tariff classification expertise, and offering inventory-financing solutions to smooth transitional disruptions. Taken together, these adjustments demonstrate how trade policy changes propagate through production planning, procurement, and product development timelines.
Unpacking source, form, application, and molecule type dimensions to reveal differentiated technical requirements and commercial pathways across the carotenoids landscape
Insightful segmentation illuminates how source, form, application, and molecular type each shape value creation and strategic choices across the carotenoids landscape. When the market is considered through the lens of source, distinctions between natural and synthetic pathways become critical: natural production pathways include microalgae cultivation, microbial fermentation, and plant extraction, each bringing unique cost structures, sustainability attributes, and quality profiles that inform buyer preferences and regulatory positioning. In parallel, differences in form-emulsion, liquid, oil suspension, and powder-directly impact formulation compatibility, shelf stability, dosing accuracy, and logistics, thereby influencing which supply options are optimal for particular end-use cases.
Application-driven segmentation highlights divergent performance and specification requirements across animal feed, cosmetics, dietary supplements, food and beverages, and pharmaceuticals, necessitating tailored quality controls, regulatory strategies, and marketing narratives for each channel. Finally, type-based differentiation among molecules such as astaxanthin, beta-carotene, canthaxanthin, lutein, lycopene, and zeaxanthin reveals varying functional attributes, extraction challenges, and clinical evidence bases, which in turn influence prioritization in R&D pipelines and commercial positioning. By synthesizing these segmentation dimensions, decision-makers can better align sourcing, formulation, and commercialization strategies to both technical constraints and market-facing opportunities.
Assessing how regional regulatory frameworks, manufacturing capabilities, and consumer preferences drive differentiated adoption, production, and traceability expectations across global markets
Regional dynamics critically shape investment, regulation, and adoption patterns for carotenoids, with distinct drivers present in the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, a combination of consumer demand for wellness products, advanced manufacturing capacity, and active venture and private-equity participation supports innovation in both natural and synthetic production routes. Meanwhile, regulatory emphasis on product claims and ingredient transparency encourages manufacturers to strengthen compliance frameworks and invest in third-party verification to satisfy informed consumers and retail partners.
In Europe, Middle East & Africa, regulatory rigor and sustainability expectations often drive premiumization and traceability requirements, prompting suppliers to document provenance and lifecycle impacts. Firms operating here frequently emphasize certified sustainable production practices and robust toxicological data. Conversely, Asia-Pacific is characterized by rapid manufacturing scale-up, a diverse supplier base, and significant investments in fermentation and algal cultivation technologies, which together position the region as both a source of cost-competitive supply and a center for process innovation. Across regions, cross-border regulatory alignment and trade policy developments continue to influence where production capacity is added and how supply chains are structured.
How companies are leveraging vertical integration, collaborative development, and compliance-driven differentiation to win formulation partners and accelerate route-to-market success
Company-level developments reflect strategic priorities such as vertical integration, platform differentiation, and value-added services that extend beyond raw material supply. Leading firms have increasingly pursued capabilities in controlled cultivation, precision fermentation, and downstream formulation support to offer customers turnkey solutions that mitigate technical risk and shorten development timelines. At the same time, partnerships between ingredient producers and end-user brands have become more common, enabling co-developed formulations that optimize stability, bioavailability, and sensory properties for specific product categories.
Commercial differentiation is also achieved through investments in quality systems, certification pathways, and data-driven traceability. These efforts not only satisfy regulatory scrutiny but also address channel-specific expectations for provenance and sustainability. Meanwhile, nontraditional entrants-such as biotechnology startups and contract research organizations-bring focused capabilities in strain engineering, process intensification, and analytical characterization, challenging incumbents to accelerate innovation and re-evaluate price-to-performance propositions. Collectively, these company-level trends point toward an ecosystem where technical excellence, compliance, and collaborative go-to-market strategies determine competitive positioning.
Practical strategic moves for industry leaders to manage supply risk, accelerate formulation innovation, and strengthen compliance-driven differentiation in carotenoids markets
Industry leaders can pursue several actionable pathways to strengthen competitive positioning and reduce execution risk in a dynamic carotenoids landscape. A primary recommendation is to diversify sourcing across production platforms-balancing microalgae, microbial fermentation, and plant-extraction suppliers-to hedge against supply shocks while capturing different sustainability and purity attributes. Complementary to this, investing in flexible formulation capabilities-capable of handling emulsion, liquid, oil suspension, and powder formats-enables rapid response to customer preferences and regulatory constraints.
Leaders should also prioritize building robust compliance and traceability systems that align with evolving regional standards, thereby facilitating smoother market entry and stronger brand trust. Strategic partnerships between ingredient providers, contract manufacturers, and end-product brands can shorten innovation cycles; therefore, creating formal collaboration frameworks that include joint development agreements and shared quality metrics will help convert R&D into commercial launches faster. Finally, allocating resources to targeted clinical and stability studies for high-value molecules such as astaxanthin, lutein, and lycopene can substantiate claims, support premium positioning, and unlock regulated channels where evidence-based differentiation is essential.
A rigorous multi-method research approach combining expert interviews, regulatory analysis, and technical literature synthesis to produce evidence-based, operationally relevant insights
The research methodology underpinning this analysis integrates primary and secondary approaches to ensure triangulation, transparency, and reproducibility. Primary inputs include interviews with technical leaders across cultivation, fermentation, and formulation teams, consultations with regulatory and quality assurance specialists, and structured discussions with commercial stakeholders in end-use industries. These interactions provide qualitative context on production constraints, specification requirements, and go-to-market dynamics that quantitative sources alone cannot fully capture.
Secondary research encompasses peer-reviewed scientific literature, regulatory guidance documents, patent filings, and industry white papers that inform understanding of technological trends, extraction and formulation advances, and safety data. Data synthesis employed cross-validation techniques to reconcile divergent perspectives and to surface consistent patterns. Throughout, emphasis was placed on documenting assumptions and methodological choices so that practitioners can interpret findings within appropriate operational and regulatory contexts. This multi-method approach supports conclusions that are both evidence-based and operationally relevant.
Synthesis of technological, regulatory, and commercial developments that will determine which organizations convert carotenoid innovation into enduring competitive advantage
In conclusion, the carotenoids landscape is being redefined by technological innovation, shifting consumer expectations, and evolving trade and regulatory environments that together influence sourcing, formulation, and commercialization strategies. Natural production pathways such as microalgae and microbial fermentation are increasingly viable alternatives to traditional extraction, offering compelling sustainability and traceability advantages, while advances in formulation formats expand applicability across food, feed, supplement, cosmetic, and pharmaceutical channels. These shifts necessitate proactive strategies around supplier diversification, compliance, and targeted evidence generation.
Looking ahead, stakeholders that integrate technical rigor with transparent sourcing narratives and collaborative development models will be better positioned to capture value and manage risk. By aligning R&D priorities with channel-specific performance requirements and by investing in quality and traceability, companies can meet rising expectations from regulators, trade partners, and consumers. Ultimately, success will favor those that combine scientific excellence with pragmatic commercial execution to translate carotenoid potential into differentiated, durable market outcomes.
Please Note: PDF & Excel + Online Access - 1 Year
Positioning carotenoids at the intersection of science, consumer demand, and industrial innovation to explain contemporary commercial and functional relevance
Carotenoids are a diverse class of pigmented compounds with critical roles across nutrition, health, and industrial applications, and they have attracted sustained interdisciplinary interest from scientists, formulators, and procurement professionals. In recent years, advances in extraction technologies, fermentation platforms, and formulation science have reshaped how carotenoids are produced and integrated into end-use applications, prompting a shift in value chains and partnerships. This introduction sets the stage by outlining essential biochemical characteristics, principal commercial types, and the functional attributes that drive application-specific demand.
Building on biochemical foundations, the narrative then considers how consumer health trends, regulatory evolutions, and manufacturing innovations converge to expand both traditional and emerging uses. Dietary supplement manufacturers emphasize bioavailability and label transparency, cosmetic brands foreground antioxidant and color stability properties, and feed formulators prioritize performance and cost-effectiveness. As a result, stakeholders across research and commercial ecosystems are rethinking sourcing strategies, due diligence frameworks, and go-to-market approaches to capture differentiated value while managing regulatory and supply-chain complexity.
How technological advances, sustainability focus, and regulatory evolution are reshaping production, formulation, and sourcing strategies across the carotenoids ecosystem
The landscape for carotenoids is undergoing transformative shifts driven by technological maturation, shifting consumer expectations, and supply-chain resilience priorities. Innovations in microalgae cultivation, precision microbial fermentation, and greener extraction chemistries are elevating the competitiveness of natural production pathways, enabling higher yields, improved purity profiles, and reduced environmental footprints. At the same time, formulation science has progressed, enabling novel delivery formats that enhance stability and bioavailability, thereby opening new application windows in functional foods and personalized nutrition.
Concurrently, consumer preferences for clean-label and sustainably sourced ingredients are prompting brand owners to demand greater traceability and provenance documentation. This dynamic is catalyzing upstream investments in traceable supply chains and third-party verification schemes. Regulatory frameworks are also evolving, tightening requirements around claims, labeling, and permissible use in certain jurisdictions. As a result, firms that couple technological capability with rigorous compliance and transparent communication are gaining differentiation, while those that rely on commoditized supply without demonstrable stewardship face reputational and operational risks.
Examining the operational and strategic ramifications of evolving United States tariffs on supply chains, sourcing decisions, and regional production incentives in 2025
Recent tariff adjustments in major markets have introduced new layers of operational complexity for manufacturers, ingredient traders, and end-product companies that depend on cross-border flows of raw materials and intermediates. Tariff changes influence sourcing strategies, push firms to reassess supplier diversification, and can alter landed costs in ways that affect formulation choices and long-term contractual arrangements. In response, many organizations have prioritized nearshoring, expanded local production capabilities, or renegotiated supplier agreements to preserve margin and continuity of supply.
Beyond immediate commercial effects, tariff-driven dynamics can accelerate structural shifts in regional value chains. For instance, increased duties on certain imported ingredients can incentivize investment in domestic fermentation or cultivation capacity, with consequential impacts on logistics, capital allocation, and workforce development. Meanwhile, trading firms and distributors have adapted by broadening their supplier base, investing in compliance and tariff classification expertise, and offering inventory-financing solutions to smooth transitional disruptions. Taken together, these adjustments demonstrate how trade policy changes propagate through production planning, procurement, and product development timelines.
Unpacking source, form, application, and molecule type dimensions to reveal differentiated technical requirements and commercial pathways across the carotenoids landscape
Insightful segmentation illuminates how source, form, application, and molecular type each shape value creation and strategic choices across the carotenoids landscape. When the market is considered through the lens of source, distinctions between natural and synthetic pathways become critical: natural production pathways include microalgae cultivation, microbial fermentation, and plant extraction, each bringing unique cost structures, sustainability attributes, and quality profiles that inform buyer preferences and regulatory positioning. In parallel, differences in form-emulsion, liquid, oil suspension, and powder-directly impact formulation compatibility, shelf stability, dosing accuracy, and logistics, thereby influencing which supply options are optimal for particular end-use cases.
Application-driven segmentation highlights divergent performance and specification requirements across animal feed, cosmetics, dietary supplements, food and beverages, and pharmaceuticals, necessitating tailored quality controls, regulatory strategies, and marketing narratives for each channel. Finally, type-based differentiation among molecules such as astaxanthin, beta-carotene, canthaxanthin, lutein, lycopene, and zeaxanthin reveals varying functional attributes, extraction challenges, and clinical evidence bases, which in turn influence prioritization in R&D pipelines and commercial positioning. By synthesizing these segmentation dimensions, decision-makers can better align sourcing, formulation, and commercialization strategies to both technical constraints and market-facing opportunities.
Assessing how regional regulatory frameworks, manufacturing capabilities, and consumer preferences drive differentiated adoption, production, and traceability expectations across global markets
Regional dynamics critically shape investment, regulation, and adoption patterns for carotenoids, with distinct drivers present in the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, a combination of consumer demand for wellness products, advanced manufacturing capacity, and active venture and private-equity participation supports innovation in both natural and synthetic production routes. Meanwhile, regulatory emphasis on product claims and ingredient transparency encourages manufacturers to strengthen compliance frameworks and invest in third-party verification to satisfy informed consumers and retail partners.
In Europe, Middle East & Africa, regulatory rigor and sustainability expectations often drive premiumization and traceability requirements, prompting suppliers to document provenance and lifecycle impacts. Firms operating here frequently emphasize certified sustainable production practices and robust toxicological data. Conversely, Asia-Pacific is characterized by rapid manufacturing scale-up, a diverse supplier base, and significant investments in fermentation and algal cultivation technologies, which together position the region as both a source of cost-competitive supply and a center for process innovation. Across regions, cross-border regulatory alignment and trade policy developments continue to influence where production capacity is added and how supply chains are structured.
How companies are leveraging vertical integration, collaborative development, and compliance-driven differentiation to win formulation partners and accelerate route-to-market success
Company-level developments reflect strategic priorities such as vertical integration, platform differentiation, and value-added services that extend beyond raw material supply. Leading firms have increasingly pursued capabilities in controlled cultivation, precision fermentation, and downstream formulation support to offer customers turnkey solutions that mitigate technical risk and shorten development timelines. At the same time, partnerships between ingredient producers and end-user brands have become more common, enabling co-developed formulations that optimize stability, bioavailability, and sensory properties for specific product categories.
Commercial differentiation is also achieved through investments in quality systems, certification pathways, and data-driven traceability. These efforts not only satisfy regulatory scrutiny but also address channel-specific expectations for provenance and sustainability. Meanwhile, nontraditional entrants-such as biotechnology startups and contract research organizations-bring focused capabilities in strain engineering, process intensification, and analytical characterization, challenging incumbents to accelerate innovation and re-evaluate price-to-performance propositions. Collectively, these company-level trends point toward an ecosystem where technical excellence, compliance, and collaborative go-to-market strategies determine competitive positioning.
Practical strategic moves for industry leaders to manage supply risk, accelerate formulation innovation, and strengthen compliance-driven differentiation in carotenoids markets
Industry leaders can pursue several actionable pathways to strengthen competitive positioning and reduce execution risk in a dynamic carotenoids landscape. A primary recommendation is to diversify sourcing across production platforms-balancing microalgae, microbial fermentation, and plant-extraction suppliers-to hedge against supply shocks while capturing different sustainability and purity attributes. Complementary to this, investing in flexible formulation capabilities-capable of handling emulsion, liquid, oil suspension, and powder formats-enables rapid response to customer preferences and regulatory constraints.
Leaders should also prioritize building robust compliance and traceability systems that align with evolving regional standards, thereby facilitating smoother market entry and stronger brand trust. Strategic partnerships between ingredient providers, contract manufacturers, and end-product brands can shorten innovation cycles; therefore, creating formal collaboration frameworks that include joint development agreements and shared quality metrics will help convert R&D into commercial launches faster. Finally, allocating resources to targeted clinical and stability studies for high-value molecules such as astaxanthin, lutein, and lycopene can substantiate claims, support premium positioning, and unlock regulated channels where evidence-based differentiation is essential.
A rigorous multi-method research approach combining expert interviews, regulatory analysis, and technical literature synthesis to produce evidence-based, operationally relevant insights
The research methodology underpinning this analysis integrates primary and secondary approaches to ensure triangulation, transparency, and reproducibility. Primary inputs include interviews with technical leaders across cultivation, fermentation, and formulation teams, consultations with regulatory and quality assurance specialists, and structured discussions with commercial stakeholders in end-use industries. These interactions provide qualitative context on production constraints, specification requirements, and go-to-market dynamics that quantitative sources alone cannot fully capture.
Secondary research encompasses peer-reviewed scientific literature, regulatory guidance documents, patent filings, and industry white papers that inform understanding of technological trends, extraction and formulation advances, and safety data. Data synthesis employed cross-validation techniques to reconcile divergent perspectives and to surface consistent patterns. Throughout, emphasis was placed on documenting assumptions and methodological choices so that practitioners can interpret findings within appropriate operational and regulatory contexts. This multi-method approach supports conclusions that are both evidence-based and operationally relevant.
Synthesis of technological, regulatory, and commercial developments that will determine which organizations convert carotenoid innovation into enduring competitive advantage
In conclusion, the carotenoids landscape is being redefined by technological innovation, shifting consumer expectations, and evolving trade and regulatory environments that together influence sourcing, formulation, and commercialization strategies. Natural production pathways such as microalgae and microbial fermentation are increasingly viable alternatives to traditional extraction, offering compelling sustainability and traceability advantages, while advances in formulation formats expand applicability across food, feed, supplement, cosmetic, and pharmaceutical channels. These shifts necessitate proactive strategies around supplier diversification, compliance, and targeted evidence generation.
Looking ahead, stakeholders that integrate technical rigor with transparent sourcing narratives and collaborative development models will be better positioned to capture value and manage risk. By aligning R&D priorities with channel-specific performance requirements and by investing in quality and traceability, companies can meet rising expectations from regulators, trade partners, and consumers. Ultimately, success will favor those that combine scientific excellence with pragmatic commercial execution to translate carotenoid potential into differentiated, durable market outcomes.
Please Note: PDF & Excel + Online Access - 1 Year
Table of Contents
187 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Growth of natural beta-carotene demand in plant-based food colorant applications due to clean label trends
- 5.2. Rising incorporation of astaxanthin derived from microalgae in nutraceuticals for ocular and cardiovascular benefits
- 5.3. Increased investment in genetically engineered microbial platforms for scalable production of rare carotenoids like lutein and zeaxanthin
- 5.4. Adoption of advanced encapsulation technologies to enhance carotenoid stability and bioavailability in functional beverages and dietary supplements
- 5.5. Strategic partnerships between agritech and biotech firms to develop biofortified crops enriched with provitamin A carotenoids under climate resilience programs
- 5.6. Expansion of personalized nutrition services offering customized carotenoid blends based on consumer genetic profiling and lifestyle data
- 5.7. Surge in application of natural astaxanthin and canthaxanthin pigments for aquaculture and poultry feed to improve animal health and product quality
- 5.8. Emergence of circular economy initiatives using fruit and vegetable waste streams for cost-effective extraction of lycopene and β-carotene
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Carotenoids Market, by Source
- 8.1. Natural
- 8.1.1. Microalgae
- 8.1.2. Microbial Fermentation
- 8.1.3. Plant Extract
- 8.2. Synthetic
- 9. Carotenoids Market, by Form
- 9.1. Emulsion
- 9.2. Liquid
- 9.3. Oil Suspension
- 9.4. Powder
- 10. Carotenoids Market, by Type
- 10.1. Astaxanthin
- 10.2. Beta-Carotene
- 10.3. Canthaxanthin
- 10.4. Lutein
- 10.5. Lycopene
- 10.6. Zeaxanthin
- 11. Carotenoids Market, by Application
- 11.1. Animal Feed
- 11.2. Cosmetics
- 11.3. Dietary Supplements
- 11.4. Food & Beverages
- 11.5. Pharmaceuticals
- 12. Carotenoids Market, by Region
- 12.1. Americas
- 12.1.1. North America
- 12.1.2. Latin America
- 12.2. Europe, Middle East & Africa
- 12.2.1. Europe
- 12.2.2. Middle East
- 12.2.3. Africa
- 12.3. Asia-Pacific
- 13. Carotenoids Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Carotenoids Market, by Country
- 14.1. United States
- 14.2. Canada
- 14.3. Mexico
- 14.4. Brazil
- 14.5. United Kingdom
- 14.6. Germany
- 14.7. France
- 14.8. Russia
- 14.9. Italy
- 14.10. Spain
- 14.11. China
- 14.12. India
- 14.13. Japan
- 14.14. Australia
- 14.15. South Korea
- 15. Competitive Landscape
- 15.1. Market Share Analysis, 2024
- 15.2. FPNV Positioning Matrix, 2024
- 15.3. Competitive Analysis
- 15.3.1. Algatech
- 15.3.2. Allied Biotech Corp. Ltd.
- 15.3.3. BASF SE
- 15.3.4. BioExtract
- 15.3.5. Chr. Hansen Holding A/S
- 15.3.6. Cyanotech Corporation
- 15.3.7. Divi’s Laboratories Ltd.
- 15.3.8. Doehler Group SE
- 15.3.9. DSM Nutritional Products AG
- 15.3.10. EID Parry Limited
- 15.3.11. Flavorchem Corporation
- 15.3.12. FMC Corporation
- 15.3.13. Fuji Chemical Industry Co. Ltd.
- 15.3.14. Givaudan SA
- 15.3.15. Kemin Industries, Inc.
- 15.3.16. LycoRed Ltd.
- 15.3.17. Novus International, Inc.
- 15.3.18. Nutralliance
- 15.3.19. Sensient Cosmetic Technologies SAS
- 15.3.20. Zhejiang Medicine Co. Ltd.
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