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144 Products found on IFF Pharma Solutions

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METHOCEL™ A4C Premium Methylcellulose - Specialty banner

IFF Pharma SolutionsMETHOCEL™ A4C Premium Methylcellulose - Specialty

Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Binder, Emulsifier
Chemical Name: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, USDA Certified, 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), 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™ A4C Premium Methylcellulose - Specialty 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™ A15 Premium LV Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Functions:Lubricant (Internal), Surfactant, Emulsifier, Mucoadhesive, Viscosity Modifier, Gelling Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Thickener, Film Former, Solubilizer, Film Former
Dosage Form:Tablets, Suspension
Labeling Claims:Dye Free, Sewage Sludge Free, Odor-free, Triphenyl Tin Compounds-Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, Gluten-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Mycotoxins-free, Pareve, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Aflatoxin-free, BSE-free, Palm Oil-free, Pesticide-free, Irradiation-free, Perfluorooctanoic Acid-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Allergen-free, Vegan, Hypoallergenic, Antibiotics-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, PVC-free, VOC-free, Melamine-free
Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), EC No. 2023/2006, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, National Formulary (NF), Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, FFDCA, European Regulation 396/2005/EC, ICH Q3C, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, EC No. 1935/2004, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), EU Directive 2002/72/EC
Manufacturing Technology:Tablet Coating, Wet Granulation, Granulation

METHOCEL™ A15 Premium LV Methylcellulose, 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.

IFF Pharma SolutionsMETHOCEL™ E10M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose, Methylcellulose
CAS Number:9004-65-3
Functions:Lubricant (Internal), Surfactant, Emulsifier, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Thickener, Film Former, Solubilizer, Film Former
Dosage Form:Capsules, Tablets, Suspension
Labeling Claims:Sewage Sludge Free, Odor-free, Quaternary Ammonium Salt-Free, Residual Solvent -Free, Halal, Tributyltin (TBT) - Free, USP 232 Elemental Impurities Free, Paraben-free, Gluten-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Perfluorocarbon (PFC)-free, Bisphenol A-free, Glycerin-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Herbicide-free, BSE-free, Palm Oil-free, Pesticide-free, No Artificial Sweeteners, Low Aldehyde, Diethylene Glycol-free, Irradiation-free, Nitrosamines-free, PFAS-Free, Impurities-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, NPE-free, CMR Substances-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Steroids Free, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Allergen-free, Vegan, Antibiotics-free, Radioactive-free, TSE-free, Kosher, Animal Products-free, Ethylene Glycol-free, Fungicide-free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Bactericide-free, Organic, Colorants-free, Plant-Based, PVC-free, VOC-free, Potassium-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 (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, National Formulary (NF), Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, European Regulation 396/2005/EC, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, FCC Compliant, USDA Organic, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), cGMP
Manufacturing Technology:Tablet Coating, Wet Granulation, Granulation

METHOCEL™ E10M Premium CR HPMC is a versatile product with various applications and functions. Ideal for tablet coating, granulation, wet granulation, tablets, and capsules, it ensures controlled and immediate release. Free from sewage sludge, it serves as a thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive, making it indispensable in pharmaceutical and nutraceutical formulations. Suitable for food containers and packaging, it boasts water solubility, ensuring quality performance in suspension formulations.

IFF Pharma SolutionsPOLYOX™ WSR N 80NF TG LEO

Chemical Name:Polyethylene Oxide
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, 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 N 80NF TG LEO, in an off-white powder form, serves as a binder and thickener in cleaning and pharmaceutical formulations. Its water solubility makes it suitable for various applications, while its direct compression manufacturing technology ensures efficient production processes. Additionally, it functions as a controlled release agent, adding value to pharmaceutical formulations.

IFF Pharma SolutionsMETHOCEL™ 228S HPMC - Specialty

Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal)
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, 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, FCC Compliant, 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), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, EU Cosmetic Regulation 1223/2009 Compliant, British Pharmacopeia (BP), Doping-Free, 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:Non-Ionic, Good Thickening Properties, 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

METHOCEL™ 228S HPMC - Specialty is a versatile pharmaceutical and nutraceutical excipient used in various dosage forms, including tablets, capsules, and suspensions. It is applied in manufacturing technologies such as tablet coating, granulation, and wet granulation. METHOCEL™ Specialty 228S HPMC functions as a controlled release agent, immediate release agent, thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive. It is water-soluble, making it an excellent choice for a range of applications.

METHOCEL™ A15 Premium LV Methylcellulose - Specialty banner

IFF Pharma SolutionsMETHOCEL™ A15 Premium LV Methylcellulose - Specialty

Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid
Chemical Name:Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
End Uses:Ceramics
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), EC No. 2023/2006, CFDA Compliant (China), Regulation (EC) No. 1333/2008, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, EC No. 1935/2004, 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, EU Directive 2002/72/EC, 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
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™ 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™ 327 Cellulose Ether - Specialty banner

IFF Pharma SolutionsMETHOCEL™ 327 Cellulose Ether - Specialty

Chemical Name:Methylcellulose, Hydroxypropyl Methylcellulose
Functions:Lubricant (Internal), Surfactant, Emulsifier, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Film Former
Labeling Claims:Steroids Free, Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Quaternary Ammonium Salt-Free, Organic, Perfluorocarbon (PFC)-free, Residual Solvent -Free, APE-free, Plant-Based, Artificial Flavor-Free, PAH-free, Antibiotics-free, VOC-free, Paraben-free, Zero Calorie, Bisphenol A-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Impurities-free, Low Odor, Kosher, PFAS-Free, Vegan, Dairy-free, Diethylene Glycol-free, No Artificial Sweeteners, Halal, Nitrosamines-free, BSE-free, PVC-free, Fungicide-free, Gluten-free, NPE-free, Herbicide-free, Mycotoxins-free, Caffeine Free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, Odor-free, PFOS-free, Allergen-free, Irradiation-free, Non-GMO, Dioxin-free, Sugar-free, Aluminum-free, Tributyltin (TBT) - Free, TSE-free, Vegetarian, Palm Oil-free, Bactericide-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, PFOA-free, Radioactive-free, Preservative-free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, GMP, Halal, Doping-Free, ISO 9001, EU Directive 2002/72/EC, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Directive 2023/2055/EU, EU Cosmetic Regulation 1223/2009 Compliant, FFDCA, Organic Certified, Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, EC No. 1935/2004, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, FDA 21 CFR 176.170, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, FCC Compliant, British Pharmacopeia (BP), FDA 21 CFR 176.180, cGMP, FDA 21 CFR 182.1480, EC No. 2023/2006, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, Regulation (EC) No. 1333/2008, EC No.1907/2006
Dosage Form:Tablets

METHOCEL™ 327 Cellulose Ether - Specialty is ideal for various pharmaceutical applications, including tablet coating, granulation, wet granulation, tablets, capsules, and suspensions. This versatile product functions as an immediate release agent, thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, mucoadhesive, and controlled release agent. It is sewage sludge-free and water-soluble, making it a reliable choice for food ingredient applications as well.

IFF Pharma SolutionsPOLYOX™ WSR - 1105 NF Grade

Chemical Name:Polyethylene Oxide
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 - 1105 NF Grade an off-white powder, serves as a binder and thickener in cleaning agents. It is available in powder form and is water-soluble, making it suitable for use in gels and osmotic pump tablets.

IFF Pharma SolutionsPOLYOX™ WSR N 750 - Specialty

Chemical Name:Pyrogenic Silica, Polyethylene Oxide, Polyethylene Glycol
Polymer Name:Polyethylene Glycol
CAS Number:25322-68-3
Chemical Family:Polyethers, Polyethylene Glycols, Ethylene Oxide Copolymers, Polyglycols, Non-Ionics

POLYOX™ WSR N 750 - Specialty, available in a white to off-white free-flowing powder with a distinctive ammoniacal odor, exhibits water solubility. Its applications in cleaning include functioning as a binder and thickener, with manufacturing often utilizing hot melt extrusion technology for its production, maintaining its physical form as a powder throughout.

IFF Pharma SolutionsPRONOVA® UP VLVG

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Halal, Biodegradable
Certifications & Compliance:ISO 14001, National Formulary (NF), Hazard Analysis Critical Control Point (HACCP), European Pharmacopeia (Ph. Eur.), ISO 9000, United States Pharmacopeia (USP), GMP, Directive 2023/2055/EU, EC No.1907/2006
Manufacturing Technology:Encapsulation

PRONOVA® UP VLVG is available in foam form with labeling claims of high purity and biodegradability. It contains sodium alginate, serves as an emulsifier and stabilizer, and is a is a modified and controlled release excipient. The product is supplied in solution form.

IFF Pharma SolutionsPOLYOX™ WSR - N80 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 - 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 - 303 FP 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 - 303 FP 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.

METHOCEL™ J12M S HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ J12M S HPMC - Specialty

Functions:Controlled Release Agent, Rheology Modifier
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Labeling Claims:Persistent Organic Pollutants (POP)-free, Natural Latex Rubber-Free, Phthalates-free, Hormones-free, Bisphenol Derivatives-free, Herbicide-free, VOC-free, Dioxane-free, TSE-free, Aflatoxin-free, Irradiation-free, PVC-free, Nitrosamines-free, APE-free, Caffeine Free, Paraben-free, Vegan, Iodide-free, Latex-free, PAH-free, Halal, Kosher, Mycotoxins-free, Sewage Sludge Free, CMR Substances-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Sugar-free, Fungicide-free, PFOA-free, Not Listed In California Proposition 65, Diethylene Glycol-free, Allergen-free, Gluten-free, Glycerin-free, Dairy-free, Organic, Monosodium Glutamate (MSG)-free, Potassium-free, Pesticide-free, Aluminum-free, Non-GMO, PFAS-Free, Ethylene Glycol-free, Vegetarian, Antibiotics-free, BSE-free, Quaternary Ammonium Salt-Free, PFOS-free, Dye Free, Palm Oil-free, Preservative-free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 10/2011 (PIM), ISO 9001, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, Regulation (EU) No. 1829/2003, ISO 50001, EC No. 1935/2004, Nagoya Compliant, FDA 21 CFR 174.5, USDA Organic, Turkish RoHS Regulation, Regulation (EC) No. 1333/2008, Halal, Directive 1333/2008/EC, FDA 21 CFR 175.300, FDA 21 CFR 175.105, Directive 2009/48/EC, FDA 21 CFR 176.180, Chinese Pharmacopeia (ChP), FDA Compliant, cGMP, ISO 14001, FSSC 22000, FDA 21 CFR 172.874, EU Directive 2002/72/EC, Generally Recognized As Safe (GRAS), European Pharmacopeia (Ph. Eur.), Clean Water Act (CWA) Certified, Swiss Ordinance (SR 817.023.21), ICH Q3C, Regulation (EU) No. 2022/1396, Organic Certified, FDA Food Safety Modernization Act (FSMA), FSC Certified, Waste Electrical & Electronic Equipment Directive (WEEE), Regulation (EU) No. 1830/2003, Regulation (EU) No. 231/2012, Kosher, FDA 21 CFR 101.9, Orthodox Union Kosher, Indian Pharmacopeia, EC No. 2023/2006, EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170
Dosage Form:Tablets

METHOCEL™ J12M S HPMC - Specialty identified as cellulose ethers and hypromellose, acts as a rheology modifier, ensuring consistency in formulations. It possesses the property of being water-soluble, making it suitable for various applications.

METHOCEL™ E5 Premium LV HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ E5 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™ E5 Premium LV HPMC - Specialty is water-soluble and used in suspensions, granulation, and tablet coating. It functions as a binder, controlled release agent, film former, and gelling agent in pharmaceuticals and nutraceuticals, and as a binder in ceramics.

IFF Pharma SolutionsMETHOCEL™ F50 HPMC - Specialty

Functions:Controlled Release Agent, Rheology Modifier
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Labeling Claims:Natural Latex Rubber-Free, Phthalates-free, Hormones-free, VOC-free, Generally Recognized As Safe (GRAS), TSE-free, Aflatoxin-free, Irradiation-free, PVC-free, Nitrosamines-free, 1,4-Dioxane-free, APE-free, Caffeine Free, Paraben-free, Vegan, PAH-free, Halal, Kosher, Mycotoxins-free, Sewage Sludge Free, CMR Substances-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Triphenyl Tin Compounds-Free, Naturally Derived, Sugar-free, Glycerin-free, Plant-Based, Dairy-free, Organic, Monosodium Glutamate (MSG)-free, Pesticide-free, Aluminum-free, Non-GMO, PFAS-Free, Vegetarian, Antibiotics-free, BSE-free, Bisphenol A-free, PFOS-free, Dye Free, Palm Oil-free, Preservative-free, Perfluorooctanoic Acid-free, Colorants-free, Plasticizer-free, Tributyl Tin Compounds-Free
Certifications & Compliance:European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), ISO 9001, RoHS 2 Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, FDA 21 CFR 182.1480, Regulation (EU) No. 1829/2003, EU Packaging Directive (94/62/EC), ISO 50001, USDA Organic, Turkish RoHS Regulation, Regulation (EC) No. 1333/2008, Halal, Directive 1333/2008/EC, Doping-Free, Directive 2009/48/EC, Majelis Ulama Indonesia Halal, Chinese Pharmacopeia (ChP), FDA Compliant, cGMP, ISO 14001, FSSC 22000, FDA 21 CFR 172.874, JECFA (FAO/WHO), European Pharmacopeia (Ph. Eur.), Swiss Ordinance (SR 817.023.21), WEEE Directive 2012/19/EU, Regulation (EU) No. 2022/1396, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2023/915/EU, Regulation (EU) No. 1830/2003, Regulation (EU) No. 231/2012, RoHS Compliant, FEMA Compliant, Kosher, FDA 21 CFR 101.9, Orthodox Union Kosher, Clean Air Act (CAA) Certified, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant
Dosage Form:Tablets

METHOCEL™ F50 HPMC - Specialty is a versatile industrial additive that serves as a rheology modifier. It belongs to the cellulose ether chemical family and is derived from plant-based hypromellose. Its water solubility makes it suitable for various applications across different industries.

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