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IFF Pharma Solutions

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154 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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METHOCEL™ K100M Premium CR HPMC banner
IFF Pharma SolutionsMETHOCEL™ K100M Premium CR HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Sustained Release Agent, Controlled Release Agent, Binder, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Suspension, Tablets
  • Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, Melamine-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-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, Allergen-free, 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
  • Certifications & Compliance:BSE & TSE, Directive 2009/48/EC, British Pharmacopeia (BP), National Bioengineered Food Disclosure Standard, 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, 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™ K100M Premium CR HPMC is utilized in suspension dosage forms and serves as a binder in ceramic industrial applications. It carries labeling claims of being caffeine-free, colorant-free, dioxin-free, dye-free, and hormone-free. With manufacturing methods such as granulation and tablet coating, it exhibits water solubility.
METHOCEL™ E50 PVC HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ E50 PVC HPMC - Specialty
  • Chemical Name:Sodium Chloride, Hydroxypropyl Methylcellulose
  • Functions:Lubricant (Internal), Surfactant, Emulsifier, Binder, Film Former, Rheology Modifier, Plasticizer, Controlled Release Agent
  • Labeling Claims:Dairy-free, Not Listed In California Proposition 65, Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Organic, Hypoallergenic, Mycotoxins-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, 1,4-Dioxane-free, Plant-Based, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, VOC-free, Paraben-free, Dioxin-free, Zero Calorie, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, Low Odor, Kosher, Preservative-free, PFAS-Free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), RoHS 2 Compliant, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, GMP, Turkish RoHS Regulation, Halal, Doping-Free, ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, RoHS Compliant, Regulation (EU) No. 1829/2003, Directive 1333/2008/EC, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FFDCA, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), EU Packaging Directive (94/62/EC), Majelis Ulama Indonesia Halal, Clean Air Act (CAA) Certified, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), FDA 21 CFR 182.1480, Orthodox Union Kosher, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, Regulation (EC) No. 1333/2008
  • Dosage Form:Tablets
METHOCEL™ E50 PVC HPMC - Specialty sourced from plants, is suitable for suspension dosage forms. It boasts labeling claims of being aluminum-free and antibiotic-free. With manufacturing technologies like granulation and tablet coating, it serves various pharmaceutical and nutraceutical functions, including mucoadhesion, solubilization, sustained release, and viscosity modification. It exhibits water solubility.
Avicel® PH - 113 banner
IFF Pharma SolutionsAvicel® PH - 113
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Tablets
  • Labeling Claims:Not Tested on Animals, Ethylene Oxide-free, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, PAH-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, Heavy Metal-free, PFAS-Free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003, IFANCA Halal, IFRA Compliant
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
Avicel® PH - 113 composed of microcrystalline cellulose, finds application in tablet formulations. Manufactured using direct compression, dry granulation, and wet granulation techniques, it serves as a binder and compression aid. Derived from non-animal sources, it meets pharmaceutical and nutraceutical standards.
METHOCEL™ 228S HPMC - Specialty banner
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.
ETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty
  • Chemical Name:Ethylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • CAS Number:9004-57-3
  • Dosage Form:Tablets
  • Labeling Claims:Dioxin-free, Paraben-free, Aflatoxin-free, Triphenyl Tin Compounds-Free, Halal, PFOS-free, Phthalates-free, Nitrosamines-free, Sugar-free, Irradiation-free, PHO (Partially Hydrogenated Oil)-Free, Palm Oil-free, APE-free, Allergen-free, Antibiotics-free, Colorants-free, TSE-free, Formaldehyde-free, Plasticizer-free, Dairy-free, BSE-free, Glycerin-free, Dye Free, Endocrine Disruptor-free, VOC-free, Hormones-free, Bisphenol A-free, PAH-free, Preservative-free, 1,4-Dioxane-free, Mycotoxins-free, Aluminum-free, Caffeine Free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, Sewage Sludge Free, Organic, Monosodium Glutamate (MSG)-free, Kosher, PFAS-Free, CMR Substances-free, Tributyl Tin Compounds-Free, Zero Calorie, PVC-free, Pesticide-free
  • Certifications & Compliance:Clean Air Act (CAA) Certified, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant, European Regulation 396/2005/EC, FDA 21 CFR 163, 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, GMP, FCC Compliant, Japan Chemical Substances Control Law (CSCL), Japan Pharmacopeia (JP), USDA Organic, Turkish RoHS Regulation, Canadian Environmental Protection Act (CEPA), Regulation (EC) No. 1333/2008, Doping-Free, Directive 2009/48/EC, Majelis Ulama Indonesia Halal, Chinese Pharmacopeia (ChP), FDA Compliant, FDA 21 CFR 181.24, cGMP, FSSC 22000, Swiss Ordinance (SR 817.023.21), ICH Q3C, EuPIA Listed, WEEE Directive 2012/19/EU, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2023/915/EU, Regulation (EU) No. 231/2012, RoHS Compliant, Kosher, FDA 21 CFR 101.9
  • Manufacturing Technology:Encapsulation, Direct Compression, Granulation, Tablet Coating
ETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty offers binding and controlled release properties along with excellent flexibility and thermal stability. It's compatible with varnishes, lacquers, and hot melt coating processes, and is soluble in ethanol.
POLYOX™ WSR - 1105 NF Grade banner
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.
POLYOX™ WSR - N80 NF Grade banner
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.
POLYOX™ WSR - 303 FP NF Grade banner
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.
ETHOCEL™ Standard 45 Premium Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 45 Premium Ethylcellulose - Specialty
  • INCI Name:Ethylcellulose
  • Ingredient Name:Ethyl Cellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Chemical Name:Ethylcellulose
  • Ingredient Origin:Plant Origin
  • CAS Number:9004-57-3
  • Labeling Claims:Caffeine Free, Irradiation-free, VOC-free, Kosher, Triphenyl Tin Compounds-Free, Mycotoxins-free, BSE-free, Bisphenol A-free, Glycerin-free, Aflatoxin-free, Zero Calorie, Vegan, TSE-free, Monosodium Glutamate (MSG)-free, Naturally Derived, Phthalates-free, Paraben-free, Non-Mutagenic, Endocrine Disruptor-free, Non-Irritant, Preservative-free, Aluminum-free, Sewage Sludge Free, Perfluorooctanoic Acid-free, Colorants-free, Vegetarian, GMO-free, PFAS-Free, Formaldehyde-free, Tributyl Tin Compounds-Free, Palm Oil-free, Dioxin-free, PAH-free, Natural Latex Rubber-Free, Organic, Allergen-free, Plant-Based, Antibiotics-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, CMR Substances-free, PVC-free, Pesticide-free, Animal Products-free, Sugar-free, 1,4-Dioxane-free, Nitrosamines-free, Plasticizer-free, Halal, Solvent-free, PFOS-free
  • Certifications & Compliance:Regulation (EU) No. 1272/2008, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant, Canadian Environmental Protection Act (CEPA), Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), US FDA Compliance Policy Guide Section 560.750, Regulation (EC) No. 1333/2008, USDA Organic, Clean Air Act (CAA) Certified, Regulation (EU) No. 1829/2003, EXCiPACT, RoHS Compliant, EC No. 1935/2004, ICH Q3D, FDA Food Safety Modernization Act (FSMA), Japan Chemical Substances Control Law (CSCL), European Regulation 396/2005/EC, RoHS 2 Compliant, FDA 21 CFR 73.1001, EuPIA Listed, Majelis Ulama Indonesia Halal, Directive 2001/18/EC, Japan Pharmacopeia (JP), FCC Compliant, United States Pharmacopeia (USP), JECFA (FAO/WHO), Regulation (EU) No. 231/2012, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1935/2004, WEEE Directive 2012/19/EU, FDA 21 CFR 573.420, Organic Certified, Halal, FDA Compliant, Turkish RoHS Regulation, Kosher, CFDA Compliant (China), FDA 21 CFR 73.1, Doping-Free, Directive 2009/48/EC, Regulation (EU) No. 1169/2011, GMP, Orthodox Union Kosher, FSSC 22000, cGMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 163, ISO 9000, Belgian Law And Codex Alimentarius Standards, Regulation (EU) No. 1830/2003, FDA 21 CFR 172.868, ICH Q3C, Hazard Analysis Critical Control Point (HACCP), FDA 21 CFR 181.24, National Formulary (NF), ISO 9001, Swiss Ordinance (SR 817.023.21), British Pharmacopeia (BP), EU Directive 2002/72/EC
ETHOCEL™ Standard 45 Premium Ethylcellulose - Specialty with its white color and powder form, offers versatile applications in tablet manufacturing. Its benefits include binding and controlled release properties, along with excellent flexibility. Utilizing direct compression or encapsulation techniques, it enables hot melt coating and is soluble in ethanol, organic solvents, and isopropanol.
METHOCEL™ A4C Methylcellulose - Specialty banner
IFF Pharma SolutionsMETHOCEL™ A4C Methylcellulose - Specialty
  • Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal)
  • Chemical Name: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, 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™ A4C Methylcellulose - Specialty a plant-derived cellulose ether, serves as a rheology modifier in various industrial processes. It is free from caffeine, colorants, dioxins, and dyes, ensuring a cleaner formulation. This versatile additive belongs to the cellulose ethers family.
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.
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.
METHOCEL™ F50 HPMC - Specialty banner
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.
METHOCEL™ E6 Premium LV Capsule Grade HPMC banner
IFF Pharma SolutionsMETHOCEL™ E6 Premium LV Capsule Grade HPMC
  • Chemical Name:Hydroxypropyl 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, 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, Hypoallergenic, 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, EC No.1907/2006, 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, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), cGMP
  • Manufacturing Technology:Tablet Coating, Wet Granulation, Granulation
METHOCEL™ E6 Premium LV Capsule Grade 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.

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