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91 Products found on IFF Pharma Solutions in Pharmaceuticals & Nutraceuticals

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IFF Pharma SolutionsMETHOCEL™ E50 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Sustained Release Agent, Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Mucoadhesive, Viscosity Modifier, Binder, Gelling Agent, Plasticizer, Controlled Release Agent, Film Former, Thickener, Immediate Release Agent, Solubilizer
Dosage Form:Tablets, Suspension
Labeling Claims:Kosher, Vegan, Zero Calorie, Colorants-free, Hypoallergenic, Pesticide-free, Allergen-free, PAH-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, USP 232 Elemental Impurities Free, Phthalates-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, PFOS-free, VOC-free, BSE-free, Organic, Antibiotics-free, Pareve, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Naturally Derived, TSE-free, PVC-free, Aluminum-free, Glycerin-free, Sugar-free, Irradiation-free, Animal Products-free, Monosodium Glutamate (MSG)-free, Odor-free, Perfluorooctanoic Acid-free, Palm Oil-free, Mycotoxins-free, Dioxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, Paraben-free, Halal, Non-GMO, Low Odor, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Regulation (EC) No. 1333/2008, Orthodox Union Kosher, Organic Certified, FDA 21 CFR 172.874, ISO 14001, Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), National Formulary (NF), EXCiPACT, USDA Organic, Regulation (EU) No. 1829/2003, Directive 2009/48/EC, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, European Regulation 396/2005/EC, FDA Compliant, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), FDA 21 CFR 182.1480, cGMP, CFDA Compliant (China), ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, FCC Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 2022/1396, Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), Regulation (EU) No. 1830/2003
Manufacturing Technology:Granulation, Tablet Coating

METHOCEL™ E50 Premium LV HPMC 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.

METHOCEL™ A15 Premium LV Methylcellulose - Specialty banner

IFF Pharma SolutionsMETHOCEL™ A15 Premium LV Methylcellulose - Specialty

Functions:Green Strength Enhancer, Film Former, Controlled Release Agent, Anti-Settling Agent, Plasticizer, Binder, Surfactant, Lubricant (Internal), Processing Aid, Emulsifier, Rheology Modifier
Chemical Name:Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
End Uses:Ceramics
Dosage Form:Tablets
Certifications & Compliance:CFDA Compliant (China), Regulation (EU) No. 1830/2003, GMP, Regulation (EC) No. 1333/2008, Indian Pharmacopeia, Hazard Analysis Critical Control Point (HACCP), Organic Certified, FDA 21 CFR 172.874, FDA 21 CFR 101.9, FDA 21 CFR 182.1480, ICH Q3C, FFDCA, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), FCC Compliant, cGMP, IFANCA Halal, FDA Food Safety Modernization Act (FSMA), USDA Organic, EU Directive 2002/72/EC, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, EC No. 1935/2004, British Pharmacopeia (BP), Doping-Free, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, EC No. 2023/2006, Regulation (EU) No. 1829/2003, Regulation (EU) No. 10/2011 (PIM), Generally Recognized As Safe (GRAS), ISO 9001, EXCiPACT, Directive 1333/2008/EC, National Formulary (NF), Orthodox Union Kosher, Regulation (EU) No. 1272/2008, FSSC 22000
Features:Cold Water Dispersible, Improved Dispersion, Improved Adhesion, High Cohesion, Low Surface Tension, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Good pH Stability, Anti-settling Properties, Low Ash Content, Thixotropic, Wide pH Range

METHOCEL™ A15 Premium LV Methylcellulose - Specialty a versatile water-soluble excipient, is used in granulation, tablet coating, and wet granulation processes. It is employed in drug delivery solutions for oral healthcare and in industrial applications for ceramics and refractory materials. It functions as a binder, disintegrant, emulsifier, and stabilizer.

METHOCEL™ F4M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F4M Modified Cellulose Food Grade - Specialty

Ingredient Name:Hydroxypropyl Methyl Cellulose (HPMC)
Chemical Name:Hydroxypropyl Methylcellulose
Ingredient Origin:Plant Origin
Functions:Controlled Release Agent, Film Former, Viscosity Modifier, Binder, Thickener
Labeling Claims:Kosher, Vegan, Zero Calorie, Colorants-free, Hypoallergenic, Pesticide-free, Generally Recognized As Safe (GRAS), PAH-free, Plant-Based, Phthalates-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, PFOS-free, VOC-free, BSE-free, Organic, Antibiotics-free, Pareve, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Naturally Derived, TSE-free, PVC-free, Aluminum-free, Glycerin-free, Sugar-free, Irradiation-free, Monosodium Glutamate (MSG)-free, Odor-free, Dairy-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, Paraben-free, Halal, Non-GMO, Low Odor, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:Japan Pharmacopeia (JP), Swiss Ordinance (SR 817.023.21), JECFA (FAO/WHO), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, Directive 1333/2008/EC, Regulation (EC) No. 1333/2008, Orthodox Union Kosher, Regulation (EU) No. 1935/2004, Organic Certified, FDA 21 CFR 172.874, ISO 14001, FDA 21 CFR 175.105, ISO 50001, EC No.1907/2006, Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170, National Formulary (NF), FDA 21 CFR 175.300, USDA Organic, Regulation (EU) No. 1829/2003, FDA 21 CFR 174.5, Directive 2001/83/EC, Directive 2009/48/EC, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, FEMA Compliant, European Regulation 396/2005/EC, FDA Compliant, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), FDA 21 CFR 176.180, FDA 21 CFR 182.1480, cGMP, Kosher, ICH Q3C, Regulation (EU) No. 1169/2011, EC No. 2023/2006, FCC Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 2022/1396, Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), REACH Exempt (Europe), Directive 2023/2055/EU, Regulation (EU) No. 1830/2003
Physical Form:Powder
Dosage Form:Tablets

METHOCEL™ F4M Modified Cellulose Food Grade - Specialty known for its water solubility, is utilized in various pharmaceutical and nutraceutical applications. It serves as a controlled release agent, film former, and gelling agent. Its manufacturing involves granulation and tablet coating processes.

IFF Pharma SolutionsMETHOCEL™ K100 Premium LVCR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Controlled Release Agent, Sustained Release Agent, Film Former, Mucoadhesive, Viscosity Modifier, Immediate Release Agent, Binder, Gelling Agent, Solubilizer
Dosage Form:Tablets, Suspension
Labeling Claims:Antibiotics-free, Pareve, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Dye Free, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), PAH-free, Plant-Based, Irradiation-free, USP 232 Elemental Impurities Free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Japan Pharmacopeia (JP), FDA 21 CFR 101.9, Swiss Ordinance (SR 817.023.21), JECFA (FAO/WHO), FEMA Compliant, European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, United States Pharmacopeia (USP), Organic Certified, FDA 21 CFR 172.874, ISO 14001, Indian Pharmacopeia, FDA 21 CFR 182.1480, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, Regulation (EU) No. 2022/1396, ABNT NBR 14725, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Granulation, Tablet Coating

METHOCEL™ K100 Premium LVCR HPMC belonging to the cellulose ether chemical family, is manufactured using granulation technology. In pharmaceuticals and nutraceuticals, it serves as a controlled release agent, film former, gelling agent, immediate release agent, and mucoadhesive, offering water solubility for diverse applications.

IFF Pharma SolutionsETHOCEL™ Standard 4 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
Dosage Form:Tablets
Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Dye Free, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, GMO-free, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), European Regulation 396/2005/EC, FDA 21 CFR 573.420, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Halal, Directive 2023/915/EU, Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Hot Melt Extrusion, Encapsulation, Direct Compression, Granulation, Tablet Coating

ETHOCEL™ Standard 4 Premium Ethylcellulose is a white powder that is soluble in ethanol and organic solvents. It provides benefits such as binding, controlled release, excellent flexibility, and thermal stability, making it highly suitable for various industrial applications where these properties are critical.

IFF Pharma SolutionsMETHOCEL™ E3 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Controlled Release Agent, Sustained Release Agent, Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Film Former, Thickener, Mucoadhesive, Viscosity Modifier, Immediate Release Agent, Binder, Gelling Agent, Solubilizer, Plasticizer
Dosage Form:Tablets, Suspension
Labeling Claims:Antibiotics-free, Pareve, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Dye Free, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Allergen-free, PAH-free, Residual Solvent -Free, Plant-Based, Irradiation-free, Animal Products-free, USP 232 Elemental Impurities Free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FDA 21 CFR 101.9, European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, United States Pharmacopeia (USP), Organic Certified, FDA 21 CFR 172.874, ISO 14001, Indian Pharmacopeia, FDA 21 CFR 182.1480, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, National Formulary (NF), FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, Regulation (EU) No. 2022/1396, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Granulation, Tablet Coating

METHOCEL™ E3 Premium LV HPMC suitable for suspensions, offers binding properties crucial for ceramic applications. With granulation and tablet coating manufacturing technologies, it ensures efficient production processes. Additionally, its water solubility makes it ideal for pharmaceutical and nutraceutical applications, serving as a binder and controlled release agent.

IFF Pharma SolutionsMETHOCEL™ E4M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Sustained Release Agent, Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Mucoadhesive, Viscosity Modifier, Binder, Gelling Agent, Plasticizer, Controlled Release Agent, Film Former, Thickener, Immediate Release Agent, Solubilizer
Dosage Form:Tablets, Suspension
Labeling Claims:Kosher, Vegan, Zero Calorie, Colorants-free, Hypoallergenic, Pesticide-free, Allergen-free, PAH-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, USP 232 Elemental Impurities Free, Phthalates-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, PFOS-free, VOC-free, BSE-free, Organic, Antibiotics-free, Pareve, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Naturally Derived, TSE-free, PVC-free, Aluminum-free, Glycerin-free, Sugar-free, Irradiation-free, Animal Products-free, Monosodium Glutamate (MSG)-free, Odor-free, Perfluorooctanoic Acid-free, Palm Oil-free, Mycotoxins-free, Dioxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, Paraben-free, Halal, Non-GMO, Low Odor, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Directive 1333/2008/EC, Regulation (EC) No. 1333/2008, Orthodox Union Kosher, Organic Certified, FDA 21 CFR 172.874, ISO 14001, Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), National Formulary (NF), EXCiPACT, USDA Organic, Regulation (EU) No. 1829/2003, Directive 2009/48/EC, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, European Regulation 396/2005/EC, FDA Compliant, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), FDA 21 CFR 182.1480, cGMP, CFDA Compliant (China), ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, FCC Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), Regulation (EU) No. 1830/2003
Manufacturing Technology:Granulation, Tablet Coating

METHOCEL™ E4M Premium CR HPMC is water-soluble and used in suspensions, granulation, and tablet coating. It serves as a binder, controlled release agent, film former, gelling agent, and immediate release agent in pharmaceuticals and nutraceuticals, and as a binder in ceramics.

IFF Pharma SolutionsMETHOCEL™ A4C Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Functions:Controlled Release Agent, Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Film Former, Thickener, Mucoadhesive, Suspending Agent, Viscosity Modifier, Binder, Gelling Agent, Solubilizer, Plasticizer
Dosage Form:Tablets
Labeling Claims:Antibiotics-free, Pareve, Gluten-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Dye Free, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Allergen-free, PAH-free, Plant-Based, Irradiation-free, Animal Products-free, USP 232 Elemental Impurities Free, Melamine-free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Japan Pharmacopeia (JP), FDA 21 CFR 101.9, European Regulation 396/2005/EC, FSSC 22000, USDA Certified, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, United States Pharmacopeia (USP), Organic Certified, FDA 21 CFR 172.874, ISO 14001, EC No.1907/2006, Indian Pharmacopeia, FDA 21 CFR 182.1480, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, National Formulary (NF), FCC Compliant, EXCiPACT, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Granulation, Tablet Coating

METHOCEL™ A4C Premium Methylcellulose manufactured using granulation technology, serves various functions in pharmaceutical and nutraceutical applications. It acts as a binder, film former, gelling agent, mucoadhesive, thickener, and viscosity modifier, ensuring optimal performance and formulation versatility.

IFF Pharma SolutionsMETHOCEL™ K200M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Sustained Release Agent, Film Former, Mucoadhesive, Viscosity Modifier, Immediate Release Agent, Binder, Gelling Agent, Solubilizer, Controlled Release Agent
Dosage Form:Tablets, Suspension
Labeling Claims:Antibiotics-free, Pareve, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Dye Free, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), PAH-free, Plant-Based, Irradiation-free, USP 232 Elemental Impurities Free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:Japan Pharmacopeia (JP), FDA 21 CFR 101.9, Swiss Ordinance (SR 817.023.21), JECFA (FAO/WHO), FEMA Compliant, European Regulation 396/2005/EC, FSSC 22000, 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, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, United States Pharmacopeia (USP), Organic Certified, FDA 21 CFR 172.874, ISO 14001, Indian Pharmacopeia, FDA 21 CFR 182.1480, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Directive 2009/48/EC, British Pharmacopeia (BP), National Bioengineered Food Disclosure Standard, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Granulation, Tablet Coating

METHOCEL™ K200M Premium CR HPMC used in ceramics and pharmaceuticals, acts as a binder and enables immediate release in suspensions and tablet coatings. It also serves as a film former, gelling agent, mucoadhesive, and solubilizer, offering versatile applications due to its water solubility.

IFF Pharma SolutionsPOLYOX™ WSR - 303 NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - 303 NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.

IFF Pharma SolutionsPOLYOX™ WSR - N60K LEO NF Grade

Chemical Name:Polyethylene Oxide, Pyrogenic Silica
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - N60K LEO NF Grade an off-white powder, offers versatile applications. Its industrial additives function as binders and thickeners, aiding in direct compression manufacturing. In pharmaceuticals, it acts as a binder and controlled release agent. Soluble in water, it suits abuse deterrent tablets & capsules, gels, and osmotic pump tablets.

IFF Pharma SolutionsPOLYOX™ WSR - N80 NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - N80 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.

IFF Pharma SolutionsPOLYOX™ WSR - 301 LEO NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - 301 LEO NF Grade characterized by its off-white color, serves as a binder and thickener in cosmetic formulations. It is available in powder form and exhibits water solubility. Its versatility extends to various dosage forms including abuse deterrent tablets & capsules, gels, and osmotic pump tablets.

IFF Pharma SolutionsPOLYOX™ WSR - N750 NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - N750 NF Grade is available in various dosage forms including gels, osmotic pump tablets, and traditional tablets. Utilizing direct compression manufacturing technology, it serves applications in both oral and topical drug delivery within the healthcare and pharmaceutical markets. With its properties as a binder and thickener, this white, water-soluble powder aids in formulation processes.

IFF Pharma SolutionsPOLYOX™ WSR - N80 LEO NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - N80 LEO NF Grade with its off-white color and powder form, exhibits versatile applications. In cosmetics, it functions as both a binder and a thickener, while in industrial additives, it serves similar purposes, offering water solubility for ease of use across various formulations.

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