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IFF Pharma Solutions

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142 Products found on IFF Pharma Solutions

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METHOCEL™ 254 HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ 254 HPMC - Specialty
  • Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal)
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Dosage Form:Tablets
  • Certifications & Compliance:ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS), RoHS Compliant, EC No. 2023/2006, RoHS 2 Compliant, Regulation (EC) No. 1333/2008, cGMP, Majelis Ulama Indonesia Halal, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, EC No. 1935/2004, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), ISO 50001, Organic Certified, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), USDA Organic, FDA 21 CFR 182.1480, FFDCA, EU Directive 2002/72/EC, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), European Regulation 396/2005/EC, EU Cosmetic Regulation 1223/2009 Compliant, Doping-Free, Clean Air Act (CAA) Certified, Turkish RoHS Regulation, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008
  • Features:Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range, Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties
METHOCEL™ 254 HPMC - Specialty sourced from plants, is recognized for its aluminum, antibiotics, APE, bisphenol A, and caffeine-free composition. It functions as a rheology modifier in industrial additives.
POLYOX™ WSR Coagulant FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant FP NF Grade
  • Chemical Name:Polyethylene Oxide, Pyrogenic Silica
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Binder, Thickener, Flocculant, Film Former, Viscosity Modifier, Lubricant, Controlled Release Agent
  • Dosage Form:Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
  • Labeling Claims:Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR Coagulant FP NF Grade is an off-white to white powder that is water soluble. It is used in dosage forms such as abuse deterrent tablets, capsules, and gels, providing essential properties for these pharmaceutical applications.
METHOCEL™ E50 Premium LV HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ E50 Premium LV HPMC - Specialty
  • Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener, Binder, Emulsifier
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • End Uses:Ceramics
  • Dosage Form:Tablets
  • Certifications & Compliance:CFDA Compliant (China), Regulation (EC) No. 1333/2008, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Organic Certified, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), USDA Organic, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, ICH Q3C, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, British Pharmacopeia (BP), EXCiPACT, Doping-Free, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS)
  • Features:Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range
METHOCEL™ E50 Premium LV HPMC - Specialty is a versatile ingredient suitable for various applications. In suspension dosage forms, it serves as a binder for ceramics, while its granulation and tablet coating manufacturing technologies make it adaptable for different production processes. With properties such as film formation, gelling, and mucoadhesion, it functions in pharmaceutical and nutraceutical applications, facilitating immediate release and solubilization when needed.
Protanal® AR - 1410 banner
IFF Pharma SolutionsProtanal® AR - 1410
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Steroids Free, No Artificial Sweeteners, Colorants-free, Copper-free, Natural Latex Rubber-Free, Naturally Derived, Halal, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, NPE-free, Pareve, Herbicide-free, Solvent-free, Perfluorocarbon (PFC)-free, Mycotoxins-free, Residual Solvent -Free, APE-free, Caffeine Free, Plant-Based, Barium-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Cobalt-free, Gold-Free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Cadmium-free, Palm Oil-free, Bactericide-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Radioactive-free, GMO-free, Kosher, Tin-free, Preservative-free, PFAS-Free, Conflict minerals-free, Nanomaterials-free, Potassium-free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FFDCA, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Protanal® AR - 1410 is a versatile powder designed for various functions in the pharmaceutical and nutraceutical industries. It serves as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid, ensuring optimal performance in formulations. Crafted to be sewage sludge-free, it meets high standards of quality and safety.
POLYOX™ WSR Coagulant NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
  • Dosage Form:Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
  • Labeling Claims:Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR Coagulant NF Grade is an off-white, water-soluble powder used in pharmaceutical and nutraceutical applications for direct compression manufacturing, functioning as a binder and controlled release agent.
POLYOX™ WSR - 301 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 301 NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
  • Dosage Form:Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
  • Labeling Claims:Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 301 NF Grade containing polyethylene oxide, is off-white in color and serves as a binder and thickener in both cosmetic and industrial applications. Additionally, it functions as a binder and controlled release agent in pharmaceuticals and nutraceuticals. It is available in powder form.
METHOCEL™ 240 HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ 240 HPMC - Specialty
  • Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal)
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Dosage Form:Tablets
  • Certifications & Compliance:Clean Water Act (CWA) Certified, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS), RoHS Compliant, RoHS 2 Compliant, Regulation (EC) No. 1333/2008, cGMP, Majelis Ulama Indonesia Halal, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), ISO 50001, Organic Certified, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), USDA Organic, FDA 21 CFR 182.1480, FFDCA, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), European Regulation 396/2005/EC, EU Cosmetic Regulation 1223/2009 Compliant, Doping-Free, Clean Air Act (CAA) Certified, Turkish RoHS Regulation, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008
  • Features:Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range, Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties
METHOCEL™ 240 HPMC - Specialty sourced from plants, is recognized for its aluminum, antibiotics, APE, bisphenol A, and caffeine-free composition. It functions as a rheology modifier in industrial additives.
ETHOCEL™ Standard 20 Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 20 Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Controlled Release Agent, Binder, Granulation Aid, Taste Masker
  • Dosage Form:Tablets
  • Labeling Claims:PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, Paraben-free, PAH-free, PFOS-free, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, 1,4-Dioxane-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, Formaldehyde-free, PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free
  • Certifications & Compliance:Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Canadian Environmental Protection Act (CEPA), Kosher, European Regulation 396/2005/EC, ICH Q3C, Clean Air Act (CAA) Certified, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, EuPIA Listed, Halal, Directive 2023/915/EU, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 573.420, Regulation (EU) No. 10/2011 (PIM), Organic Certified, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, FDA 21 CFR 172.868, Regulation (EU) No. 1272/2008, FDA 21 CFR 73.1001, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, FCC Compliant, FDA 21 CFR 163, USDA Organic, EXCiPACT, FDA 21 CFR 73.1, Directive 2009/48/EC, British Pharmacopeia (BP)
  • Manufacturing Technology:Tablet Coating, Hot Melt Extrusion, Direct Compression, Granulation, Encapsulation
ETHOCEL™ Standard 20 Premium Ethylcellulose White powder for binding, controlled release, flexibility, and thermal stability. Ideal for hot melt coating tablets, it is soluble in organic solvents and ethanol. It aids in granulation and acts as a taste masking agent. Suitable for direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating.
METHOCEL™ K100M Premium HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ K100M Premium HPMC - Specialty
  • Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener, Binder, Emulsifier
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • End Uses:Ceramics
  • Dosage Form:Tablets
  • Certifications & Compliance:CFDA Compliant (China), Regulation (EC) No. 1333/2008, National Bioengineered Food Disclosure Standard, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Swiss Ordinance (SR 817.023.21), Organic Certified, FEMA Compliant, Chinese Pharmacopeia (ChP), WEEE Directive 2012/19/EU, European Pharmacopeia (Ph. Eur.), USDA Organic, Kosher, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, ICH Q3C, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, JECFA (FAO/WHO), EU Cosmetic Regulation 1223/2009 Compliant, British Pharmacopeia (BP), EXCiPACT, Doping-Free, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008, Directive 2023/915/EU, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS)
  • Features:Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range
METHOCEL™ K100M Premium HPMC - Specialty is employed in ceramics as a binder, utilizing granulation in its manufacturing process. Within pharmaceuticals and nutraceuticals, it serves as a suspension aid, thickener, and viscosity modifier, boasting water solubility for versatile application.
METHOCEL™ K4M Premium HPMC banner
IFF Pharma SolutionsMETHOCEL™ K4M Premium HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Controlled Release Agent, Suspending Agent, Binder, Thickener, Mucoadhesive, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Tablets
  • Labeling Claims:VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ K4M Premium HPMC utilized in ceramics and pharmaceuticals, serves as a binder, film former, gelling agent, mucoadhesive, solubilizer, and suspension aid. It aids in granulation and exhibits water solubility.
SeaGel® CAP - 201 banner
IFF Pharma SolutionsSeaGel® CAP - 201
  • Chemical Name:Carrageenan
  • Functions:Encapsulant, Controlled Release Agent
  • Labeling Claims:Organic, Paraben-free, PFOA-free, Phthalates-free, Non-GMO, Not Listed In California Proposition 65, Fungicide-free, Dye Free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Environmentally Friendly, Natural, Plant-Based, Iodide-free, Aluminum-free, PAH-free, TSE-free, Sustainable, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Bisphenol Derivatives-free, Herbicide-free, Palm Oil-free, APE-free, Clean Label, Tributyltin (TBT) - Free, Preservative-free, Kosher, Sugar-free, Hormones-free, Potassium-free, Naturally Derived, PFAS-Free, Quaternary Ammonium Salt-Free, Vegetarian, Nitrosamines-free, Antibiotics-free, Doping Substances-free, Animal Products-free, Plasticizer-free, Dioxane-free, Allergen-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free, Gluten-free
  • Certifications & Compliance:Directive 1333/2008/EC, Regulation (EU) No. 1829/2003, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, FSSC 22000, ISO 9001, cGMP, Regulation (EU) No. 1272/2008, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Directive 396/2005/EC, FDA 21 CFR 177.1520, Clean Water Act (CWA) Certified, Nagoya Compliant, Orthodox Union Kosher, FDA 21 CFR 179.26
  • Dosage Form:Capsules
SeaGel® CAP - 201 identified as carrageenan, offers versatility and quality in capsule applications. With its natural and non-animal plant origins, it ensures ethical sourcing. Featuring easy-to-use powder form, it boasts film-forming properties, heat, and thermal stability. Additionally, it functions as an encapsulant and controlled release agent, providing enhanced performance in encapsulation processes.

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