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203 Products found on IFF Pharma Solutions

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IFF Pharma SolutionsMETHOCEL™ A4C Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Functions:Rheology Modifier, Plasticizer, Controlled Release Agent, Lubricant (Internal), Suspending Agent, Surfactant, Emulsifier, Binder, Thickener, Mucoadhesive, Film Former, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
Dosage Form:Tablets
Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, Melamine-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-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, Gluten-free, PAH-free, 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, Animal Products-free, 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:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), FFDCA, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FSSC 22000, FDA Food Safety Modernization Act (FSMA), USDA Certified, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Granulation

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 SolutionsETHOCEL™ Medium 50 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Controlled Release Agent, Binder, Granulation Aid, Taste Masker
Dosage Form:Tablets
Labeling Claims:VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, Paraben-free, PAH-free, PFOS-free, Ethylene Oxide-free, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Antibiotics-free, 1,4-Dioxane-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, Formaldehyde-free, PVC-free, Perfluorooctanoic Acid-free
Certifications & Compliance:FDA 21 CFR 73.1, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Canadian Environmental Protection Act (CEPA), EC No. 2023/2006, Kosher, European Regulation 396/2005/EC, ICH Q3C, Clean Air Act (CAA) Certified, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, EuPIA Listed, EC No. 1935/2004, Halal, Directive 2023/915/EU, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 573.420, Regulation (EU) No. 10/2011 (PIM), Organic Certified, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, FDA 21 CFR 172.868, Regulation (EU) No. 1272/2008, FDA 21 CFR 73.1001, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, FCC Compliant, FDA 21 CFR 163, USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Hot Melt Extrusion, Direct Compression, Granulation, Encapsulation

ETHOCEL™ Medium 50 Premium Ethylcellulose offers binding, controlled release, flexibility, and thermal stability. It serves as a stabilizer and thickener in cosmetics. Compatible with various manufacturing processes like direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating. It dissolves in organic solvents like ethanol and isopropanol.

IFF Pharma SolutionsPOLYOX™ WSR N 750 B4 - Specialty

Polymer Name:Polyethylene Glycol
Chemical Family:Polyglycols, Ethylene Oxide Copolymers, Non-Ionics, Polyethers, Polyethylene Glycols

POLYOX™ WSR N 750 B4 - Specialty is a versatile product with various applications in different industries. It functions as a film former, binder, and foam stabilizer, offering benefits like dense foam and excellent wet tack. This off-white to white powder is compatible with a wide range of polymers and resins, making it suitable for diverse formulations. Its features include water solubility, crosslinkability, and a high molecular weight. POLYOX™ Specialty WSR N - 750 B4 is available for your manufacturing needs, whether in the agrochemical, cosmetic, food, industrial, or pharmaceutical sectors.

IFF Pharma SolutionsETHOCEL™ Standard 7 Premium Ethylcellulose

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

ETHOCEL™ Standard 7 Premium Ethylcellulose White Powder has binding, controlled release, flexibility, and thermal stability benefits. It's soluble in organic solvents and ethanol. Used in direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating. It functions as a controlled release agent, granulation aid, and taste masking agent.

IFF Pharma SolutionsProtacid® F120 NM

Chemical Name:Alginic Acid, Algin
CAS Number:9005-38-3
Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-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, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, Directive 2001/18/EC, GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP)

Protacid® F120 NM is free from dyes, hormones, monosodium glutamate (MSG), natural latex rubber, polycyclic aromatic hydrocarbons (PAHs), and parabens. Its chemical name is algin.

IFF Pharma SolutionsPOLYOX™ WSR N 3000 H - Specialty

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

POLYOX™ WSR N 3000 H - Specialty an off-white powder, suits abuse deterrent tablets, gels, and osmotic pump tablets. It's compatible with polystyrene and used in ceramics, paper tissue, and paper toweling, offering flexibility, toughness, and resistance to grease and oil. Its viscoelastic properties and lubricity enhance its performance, along with its water solubility.

IFF Pharma SolutionsPOLYOX™ WSR - 301 FP 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, 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 - 301 FP 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 301 - Specialty

Chemical Name: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 301 - Specialty a white powder, is used in gels, osmotic pump tablets, and regular tablets. It offers viscoelasticity, lubricity, and a silky feel, making it suitable for sprayers, tissue, and toweling. It's water-soluble, compatible with polystyrene and polycaprolactone, and non-toxic.

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 SolutionsProtanal® LF - 120M

Chemical Name:Sodium Alginate
Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-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, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Chemical Inventories:ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)

Protanal® LF - 120M sourced from non-animal origins, aligns with modern labeling preferences, being free from aluminum, antibiotics, and APE. Its multifunctionality in pharmaceuticals and nutraceuticals includes serving as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, offering versatility in various applications.

IFF Pharma SolutionsProtanal® LF - 10/60LS

Chemical Name:Sodium Alginate
Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-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, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Chemical Inventories:ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)

Protanal® LF - 10/60LS available in powdered form, offers versatile applications in pharmaceuticals and nutraceuticals. It serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, providing multifunctional support in various formulations.

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™ F4M Premium HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F4M Premium HPMC - Specialty

Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener, Binder, Emulsifier
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
End Uses:Ceramics
Dosage Form:Tablets
Certifications & Compliance:CFDA Compliant (China), Regulation (EC) No. 1333/2008, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Swiss Ordinance (SR 817.023.21), Organic Certified, FEMA Compliant, Chinese Pharmacopeia (ChP), WEEE Directive 2012/19/EU, European Pharmacopeia (Ph. Eur.), USDA Organic, Kosher, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, ICH Q3C, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, JECFA (FAO/WHO), EU Cosmetic Regulation 1223/2009 Compliant, British Pharmacopeia (BP), EXCiPACT, Doping-Free, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008, Directive 2023/915/EU, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS)
Features:Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range

METHOCEL™ F4M Premium HPMC - Specialty is water-soluble and finds application in ceramics and pharmaceuticals. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, suspension aid, thickener, and viscosity modifier. Produced through granulation, it serves various industrial and pharmaceutical functions.

METHOCEL™ K4M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K4M Modified Cellulose Food Grade - Specialty

Chemical Name:Hydroxypropyl Methylcellulose
Functions:Controlled Release Agent
Labeling Claims:Dairy-free, 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, Pareve, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Plant-Based, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), 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, Tributyl Tin Compounds-Free, Low Odor, Kosher, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, JECFA (FAO/WHO), GMP, FEMA Compliant, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Swiss Ordinance (SR 817.023.21), Directive 1333/2008/EC, Directive 2023/2055/EU, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, 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, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, FDA 21 CFR 176.180, FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), cGMP, FSSC 22000, FDA 21 CFR 182.1480, Orthodox Union Kosher, 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™ K4M Modified Cellulose Food Grade - Specialty a food-grade product, acts as a binder, controlled release agent, film former, and gelling agent in pharmaceuticals and nutraceuticals. It facilitates granulation and tablet coating processes and exhibits water solubility.

IFF Pharma SolutionsAquacoat® ECD - 30

Chemical Name:Ethylcellulose
Dosage Form:Tablets
Labeling Claims:Paraben-free, Phthalates-free, Tributyl Tin Compounds-Free, Ethylene Oxide-free, Triphenyl Tin Compounds-Free, Non-GMO, Not Listed In California Proposition 65, Dye Free, GMO-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, Colorants-free, Not Tested on Animals, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Aluminum-free, Melamine-free, PAH-free, TSE-free, Amine-free, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Genotoxic-free, Palm Oil-free, Dioxin-free, APE-free, Preservative-free, Kosher, Nanomaterials-free, Bisphenol A-free, Sugar-free, Hormones-free, PFAS-Free, Vegetarian, Perfluorooctanoic Acid-free, Nitrosamines-free, Antibiotics-free, Heavy Metal-free, Plasticizer-free, Allergen-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free, Latex-free
Certifications & Compliance:EXCiPACT, Regulation (EU) No. 231/2012, Chinese Pharmacopeia (ChP), European Regulation 396/2005/EC, FSSC 22000, cGMP, European Pharmacopeia (Ph. Eur.), GMP, FCC Compliant, Doping-Free, Japan Pharmacopeia (JP), United States Pharmacopeia (USP), British Pharmacopeia (BP), IFANCA Halal, FDA Food Safety Modernization Act (FSMA), National Formulary (NF), Nagoya Compliant, Orthodox Union Kosher, FDA Compliant, FDA 21 CFR Regulations

Aquacoat® ECD - 30 containing ethylcellulose, is a liquid formulation utilized for tablet coating. With labeling claims of being palm oil-free, glycerin-free, and endocrine disruptor-free, it serves as a controlled release agent, enteric coating system, sustained release agent, and taste masking agent in pharmaceutical and nutraceutical applications.

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