IFF Pharma Solutions

252 Products found on IFF Pharma Solutions in Excipients

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TDSWith TDS

IFF Pharma SolutionsProtanal® LF - 200FTS

Chemical Name:Sodium Alginate
Ingredient Name:Sodium Alginate
CAS Number:9005-38-3
Labeling Claims:PVC-free, Melamine-free, Gold-Free, PFAS-Free, Potassium-free, Impurities-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, NPE-free, CMR Substances-free, Plasticizer-free, Nanomaterials-free, Copper-free, Barium-free, APE-free, Quaternary Ammonium Salt-Free, Vegetarian, Residual Solvent -Free, Halal, Tributyltin (TBT) - Free, Paraben-free, Gluten-free, Cadmium-free, Propylene Glycol-free, PAH-free, Steroids Free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Caffeine Free, Tin-free, Perfluorocarbon (PFC)-free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, Latex-free, Radioactive-free, Aflatoxin-free, TSE-free, Mercury-Free, Herbicide-free, Kosher, Animal Products-free, Fungicide-free, Hormones-free, BSE-free, Palm Oil-free, Solvent-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Bactericide-free, No Artificial Sweeteners, Colorants-free, Irradiation-free, Cobalt-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FFDCA, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, European Regulation 396/2005/EC, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, FDA 21 CFR 117, European Pharmacopeia (Ph. Eur.), IFRA Compliant, EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), ISO 14001, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ISO 9000, EXCiPACT
Chemical Inventories:AICS (Australia), NDSL (Canada), ECL (Korea), PICCS (Phillipines), ENCS (Japan), IECSC (China), DSL (Canada)

Protanal® LF- 200FTS is a versatile powder designed for various applications in food ingredients, pharmaceuticals, and nutraceuticals. This product boasts features like being sewage-sludge-free, ensuring purity and safety. It functions as a controlled release agent, gelling agent, thickener, and stabilizer, offering multifunctionality. In pharmaceuticals and nutraceuticals, it also serves as an antacid, providing added value.

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.

POLYOX™ WSR 301 LEO NF Grade - Specialty banner

IFF Pharma SolutionsPOLYOX™ WSR 301 LEO NF Grade - Specialty

INCI Name:PEG-90M
Chemical Name:Polyethylene Oxide
Chemical Family:Cellulose Ethers, Ethylene Oxide Copolymers, Cellulose & Cellulosics
Ingredient Origin:Plant Origin, Synthetic, Non-Animal Origin
Labeling Claims:Oxidatively Degradable, TSE-free, Ethylene Glycol-free, Vegetarian, Zinc-free, Plant-Based, Not Tested on Animals, Nitrosamines-free, Kosher, BSE-free, Chlorine-free, Ethylene Oxide-free, Irradiation-free, Animal Products-free, No Added Formaldehyde, Diethylene Glycol-free, Halal, Allergen-free, Dairy-free, Non-GMO, Vegan, Heavy Metal-free, Residual Solvent -Free, Naturally Derived

POLYOX™ WSR 301 LEO NF Grade - Specialty 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.

METHOCEL™ 10-0352 Cellulose Ether - Specialty banner

IFF Pharma SolutionsMETHOCEL™ 10-0352 Cellulose Ether - Specialty

Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Binder, Emulsifier
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
Certifications & Compliance:EC No. 2023/2006, Regulation (EC) No. 1333/2008, FDA 21 CFR 176.170, cGMP, GMP, Directive 2023/2055/EU, 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, EC No.1907/2006, FDA Compliant, Regulation (EU) No. 1169/2011, FDA 21 CFR 175.105, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, FDA 21 CFR 175.300, FDA 21 CFR 176.180, EU Cosmetic Regulation 1223/2009 Compliant, British Pharmacopeia (BP), FDA 21 CFR 174.5, 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 2001/83/EC, Regulation (EU) No. 1935/2004, 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, Good pH Stability, Wide pH Range

METHOCEL™ 10-0352 Cellulose Ether - Specialty is a versatile excipient used in pharmaceutical applications. It functions as a controlled release agent, immediate release agent, thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive. Suitable for use in tablets, capsules, and suspensions, it is also effective in tablet coating, granulation, and wet granulation processes. This water-soluble cellulose ether offers benefits such as zero calorie content and low odor.

IFF Pharma SolutionsPOLYOX™ WSR - 303 NF TG LEO

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 NF TG LEO featuring an off-white color and a powder physical form, serves as a binder and thickener in various cleaning applications. It is formulated for use in gels, osmotic pump tablets, and conventional tablets, offering water solubility for effective performance.

IFF Pharma SolutionsAvicel® PH - 112

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Granules, Tablets, Suspension
Labeling Claims:Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Not Tested on Animals, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Genotoxic-free, Ethylene Glycol-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, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Kosher, Amine-free, Dioxane-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, 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), Nagoya Compliant, ISO 45001, cGMP, ABNT NBR 14725, 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
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® PH - 112 is used in direct compression, dry granulation, and wet granulation applications. It is caffeine-free, CMR substance-free, diethylene glycol-free, and dioxane-free, ensuring safe and effective pharmaceutical formulations.

IFF Pharma SolutionsETHOCEL™ Standard 10 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 10 Premium Ethylcellulose characterized by its white color, serves as a stabilizer and thickener in cosmetic ingredients. Utilizing encapsulation, granulation, hot melt extrusion, and tablet coating technologies, it is available in a powdered physical form.

IFF Pharma SolutionsMETHOCEL™ E50 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Lubricant (Internal), Surfactant, Emulsifier, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Sustained Release 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, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-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, Not Listed In California Proposition 65, 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
Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), 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, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, European Regulation 396/2005/EC, ICH Q3C, 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)
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ E50 Premium LV HPMC is a versatile ingredient suitable for various applications. In suspension dosage forms, it serves as a binder for ceramics, while its granulation and tablet coating manufacturing technologies make it adaptable for different production processes. With properties such as film formation, gelling, and mucoadhesion, it functions in pharmaceutical and nutraceutical applications, facilitating immediate release and solubilization when needed.

IFF Pharma SolutionsMETHOCEL™ K100 Premium LVCR 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: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, 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, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Regulation (EU) No. 2022/1396, ABNT NBR 14725, USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Granulation

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

IFF Pharma SolutionsMETHOCEL™ VLV Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Controlled Release Agent, Coating System, Binder, Thickener, Solubilizer, Film Former
Dosage Form:Capsules, Tablets, Suspension, Orally Disintegrating Films (ODFs), Granules
Labeling Claims:Sewage Sludge Free, Odor-free, Quaternary Ammonium Salt-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, Palm Oil-free, Solvent-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, FSSC 22000, Steroids Free, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Residues-free, Allergen-free, Vegan, Antibiotics-free, Radioactive-free, Kosher, Ethylene Glycol-free, Fungicide-free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Bactericide-free, Organic, Colorants-free, Plant-Based, PVC-free, Non-Toxic, VOC-free, Persistent Organic Pollutants (POP)-free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), FDA 21 CFR 174.5, JECFA (FAO/WHO), EC No. 2023/2006, SCF Listed, 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, Regulation (EU) No. 1272/2008, EU Cosmetic Regulation 1223/2009 Compliant, European Parliament and Council Directive (E464), FDA 21 CFR 176.170, Regulation (EU) No. 1935/2004, National Formulary (NF), FDA 21 CFR 175.300, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, Kosher, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, FDA 21 CFR 176.180, EC No. 1935/2004, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, FDA 21 CFR 175.105, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Directive 2012/19/EU, Regulation (EU) No. 1169/2011, FCC Compliant, Regulations (EU) No. 1129/2011, USDA Organic, EXCiPACT, Directive 2011/62/EU, EFSA (European Food Safety Authority) Certified, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), EU Directive 2002/72/EC, cGMP
Manufacturing Technology:Tablet Coating, Wet Granulation

METHOCEL™ VLV Premium HPMC is a versatile industrial additive designed for various applications, including tablet coating, orally disintegrating films, capsules, suspensions, and granules. With high efficiency and water solubility, it offers excellent cohesion development, green strength, and water retention. It functions as a binder, emulsifier, lubricant, and surfactant make it indispensable across manufacturing processes. Additionally, it serves as a water retention agent, binder and resin, slip agent, coating system, mucoadhesive, film former, viscosity modifier, solubilizer, gelling agent, and immediate release agent. METHOCEL™ VLV Premium HPMC's improved pumpability and lubricating properties ensure easy handling, making it a go-to choice for industrial and pharmaceutical formulations.

IFF Pharma SolutionsAvicel® PH - 301

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Granules, Tablets, Suspension
Labeling Claims:Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Not Tested on Animals, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Genotoxic-free, Ethylene Glycol-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, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Kosher, Amine-free, Dioxane-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, 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), Nagoya Compliant, ISO 45001, cGMP, ABNT NBR 14725, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® PH - 301 is a multifunctional ingredient utilised in various pharmaceutical applications, including granules, suspensions, and tablets. It acts as a binder, compression aid, filler, and immediate release agent, streamlining the manufacturing process and ensuring consistent product quality. This versatile component enhances formulation efficiency and contributes to the development of high-performance pharmaceutical products.

IFF Pharma SolutionsProtanal® PH - 1033

Chemical Name:Sodium Alginate
Ingredient Name:Sodium Alginate
CAS Number:9005-38-3
Labeling Claims:PVC-free, Melamine-free, Gold-Free, PFAS-Free, Potassium-free, Impurities-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, NPE-free, CMR Substances-free, Plasticizer-free, Nanomaterials-free, Copper-free, Barium-free, APE-free, Quaternary Ammonium Salt-Free, Vegetarian, Residual Solvent -Free, Halal, Tributyltin (TBT) - Free, Paraben-free, Gluten-free, Cadmium-free, Propylene Glycol-free, PAH-free, Steroids Free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Caffeine Free, Tin-free, Perfluorocarbon (PFC)-free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, Latex-free, Radioactive-free, Aflatoxin-free, TSE-free, Mercury-Free, Herbicide-free, Kosher, Animal Products-free, Fungicide-free, Hormones-free, BSE-free, Palm Oil-free, Solvent-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Bactericide-free, No Artificial Sweeteners, Colorants-free, Irradiation-free, Cobalt-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FFDCA, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, European Regulation 396/2005/EC, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, FDA 21 CFR 117, European Pharmacopeia (Ph. Eur.), IFRA Compliant, EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), ISO 14001, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ISO 9000, EXCiPACT
Chemical Inventories:AICS (Australia), NDSL (Canada), PICCS (Phillipines), ENCS (Japan), IECSC (China), DSL (Canada)

Protanal® PH - 1033 is a versatile powder free from sewage sludge. Ideal for pharmaceuticals and nutraceuticals, it serves as a controlled release agent, gelling agent, thickener, and stabilizer. Plus, it offers antacid properties, ensuring top-notch performance in various applications.

IFF Pharma SolutionsProtanal® LF - 10/60

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), 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 - 10/60 composed of sodium alginate, originates from non-animal sources. It serves various functions in pharmaceuticals and nutraceuticals, including as an antacid, controlled release agent, gelling agent, and thickener, available in powder form.

IFF Pharma SolutionsManucol® LD

Chemical Name:Sodium Alginate
Labeling Claims:Not Listed In California Proposition 65, Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-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, 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, 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, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Chemical Inventories:TSCA (USA), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)

Manucol® LD composed of sodium alginate, serves various pharmaceutical and nutraceutical functions, including antacid properties, controlled release, gelling, stabilization, and thickening.

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.

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