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IFF Pharma Solutions

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152 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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METHOCEL™ 327 Cellulose Ether - Specialty banner
IFF Pharma SolutionsMETHOCEL™ 327 Cellulose Ether - Specialty
  • INCI Name:Methylcellulose
  • Chemical Name:Methylcellulose, Hydroxypropyl Methylcellulose
  • Dosage Form:Tablets
  • Labeling Claims:Kosher, Steroids Free, Vegan, Zero Calorie, Artificial Flavor-Free, Colorants-free, Diethylene Glycol-free, Fungicide-free, Pesticide-free, PAH-free, Allergen-free, Residual Solvent -Free, Plant-Based, Radioactive-free, Phthalates-free, PHO (Partially Hydrogenated Oil)-Free, NPE-free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Quaternary Ammonium Salt-Free, PFOS-free, VOC-free, BSE-free, Organic, Antibiotics-free, Pareve, Gluten-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Bactericide-free, Naturally Derived, TSE-free, PVC-free, Aluminum-free, Perfluorocarbon (PFC)-free, Glycerin-free, Sugar-free, Ethylene Glycol-free, Irradiation-free, Animal Products-free, Monosodium Glutamate (MSG)-free, Odor-free, Dairy-free, Palm Oil-free, CMR Substances-free, No Artificial Sweeteners, Mycotoxins-free, Dioxin-free, Herbicide-free, Preservative-free, APE-free, PFOA-free, Impurities-free, Paraben-free, Tributyltin (TBT) - Free, Halal, Non-GMO, Low Odor, Sewage Sludge Free, Plasticizer-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 (EC) No. 1333/2008, Orthodox Union Kosher, Regulation (EU) No. 1935/2004, FDA 21 CFR 172.874, Organic Certified, ISO 14001, FDA 21 CFR 175.105, ISO 50001, EC No.1907/2006, Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170, National Formulary (NF), FDA 21 CFR 175.300, USDA Organic, Regulation (EU) No. 1829/2003, FDA 21 CFR 174.5, Directive 2001/83/EC, Directive 2009/48/EC, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, European Regulation 396/2005/EC, EC No. 1935/2004, FDA Compliant, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), FDA 21 CFR 182.1480, FDA 21 CFR 176.180, cGMP, Regulation (EU) No. 1169/2011, FFDCA, Halal, Quality Control BV Netherlands, EC No. 2023/2006, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 2022/1396, Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), Directive 2023/2055/EU, EU Directive 2002/72/EC, Regulation (EU) No. 1830/2003
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.
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:PFOS-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, Vegan, GMO-free, Zero Calorie, Plant-Based, Mycotoxins-free, Pesticide-free, Hormones-free, APE-free, Sugar-free, Perfluorooctanoic Acid-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, PHO (Partially Hydrogenated Oil)-Free, Animal Products-free, Glycerin-free, Paraben-free, Phthalates-free, Formaldehyde-free, 1,4-Dioxane-free, PAH-free, Halal, PVC-free, Aluminum-free, PFAS-Free, Antibiotics-free, Aflatoxin-free, Non-Irritant, Non-Mutagenic, Caffeine Free, Organic, Irradiation-free, VOC-free, Endocrine Disruptor-free, Vegetarian, Tributyl Tin Compounds-Free, Allergen-free, Solvent-free, Natural Latex Rubber-Free, Nitrosamines-free, TSE-free, Non-GMO, Naturally Derived, Kosher, CMR Substances-free, Colorants-free, Sewage Sludge Free, Dye Free, Dioxin-free, Preservative-free, Palm Oil-free, BSE-free
  • Certifications & Compliance:FDA 21 CFR 163, EXCiPACT, Indian Pharmacopeia, Regulation (EU) No. 10/2011 (PIM), EU Cosmetic Regulation 1223/2009 Compliant, Canadian Environmental Protection Act (CEPA), Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, US FDA Compliance Policy Guide Section 560.750, Regulation (EU) No. 1829/2003, FDA 21 CFR 573.420, Orthodox Union Kosher, Clean Air Act (CAA) Certified, RoHS Compliant, Japan Chemical Substances Control Law (CSCL), European Regulation 396/2005/EC, RoHS 2 Compliant, EC No. 1935/2004, Regulation (EU) No. 1830/2003, Directive 2001/18/EC, cGMP, Japan Pharmacopeia (JP), FCC Compliant, Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), JECFA (FAO/WHO), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, WEEE Directive 2012/19/EU, Organic Certified, Regulation (EU) No. 1272/2008, Majelis Ulama Indonesia Halal, Halal, FDA Compliant, Turkish RoHS Regulation, CFDA Compliant (China), Doping-Free, USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, Kosher, Regulation (EU) No. 1169/2011, ICH Q3C, GMP, EuPIA Listed, ICH Q3D, FSSC 22000, Regulation (EC) No. 1333/2008, ISO 9000, Belgian Law And Codex Alimentarius Standards, EC No.1907/2006, Swiss Ordinance (SR 817.023.21), FDA 21 CFR 172.868, Hazard Analysis Critical Control Point (HACCP), Generally Recognized As Safe (GRAS), FDA 21 CFR 181.24, National Formulary (NF), ISO 9001, 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.
Protacid® AR - 8640 banner
IFF Pharma SolutionsProtacid® AR - 8640
  • Chemical Name:Alginic Acid
  • CAS Number:9005-32-7
  • Functions:Antacid, Controlled Release Agent
  • Labeling Claims:Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Dye Free, Kosher, Propylene Glycol-free, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), Solvent-free, PAH-free, Allergen-free, Residual Solvent -Free, Irradiation-free, Animal Products-free, Melamine-free, Latex-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, BSE-free, Paraben-free, Halal, Non-GMO, GMO-free, Nanomaterials-free, Plasticizer-free, Antibiotics-free, Pareve
  • Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), ISO 14001, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Kosher, National Formulary (NF), Halal Food Council of Europe, EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, ISO 9000, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, Regulation (EU) No. 1830/2003
Protacid® AR - 8640 belongs to the chemical family of alginates, specifically alginic acid. In pharmaceutical and nutraceutical applications, it serves as both an antacid and a controlled-release agent.
POLYOX™ WSR - N12K NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N12K NF Grade is an off-white powder with water-soluble properties. It's used as a binder and thickener in cleaning products and pharmaceuticals. Its applications include gels, osmotic pump tablets, and regular tablets, and it's manufactured using direct compression technology. Additionally, it serves as a controlled release agent.
Manucol® LD banner
IFF Pharma SolutionsManucol® LD
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Palm Oil-free, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free, Halal, Paraben-free, Aluminum-free
  • Certifications & Compliance:IFRA Compliant, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Chinese Pharmacopeia (ChP), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008
  • Chemical Inventories:PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), TSCA (USA)
Manucol® LD composed of sodium alginate, serves various pharmaceutical and nutraceutical functions, including antacid properties, controlled release, gelling, stabilization, and thickening.
POLYOX™ WSR - 205 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 205 NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 205 NF Grade characterized by its off-white color, is available in powder form. It serves as a binder and thickener in various industrial applications. Its water solubility makes it suitable for abuse deterrent tablets and capsules, 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), Film Former, Flocculant, Binder, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N80 NF Grade is an off-white to white powder that is water soluble. It is used in dosage forms such as abuse deterrent tablets, capsules, and gels, providing essential properties for these pharmaceutical applications.

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