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IFF Pharma Solutions

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112 Products found on IFF Pharma Solutions

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POLYOX™ WSR N 80NF TG LEO banner
IFF Pharma SolutionsPOLYOX™ WSR N 80NF TG LEO
  • 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 N 80NF TG LEO, in an off-white powder form, serves as a binder and thickener in cleaning and pharmaceutical formulations. Its water solubility makes it suitable for various applications, while its direct compression manufacturing technology ensures efficient production processes. Additionally, it functions as a controlled release agent, adding value to pharmaceutical formulations.
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), 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 - 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.
POLYOX™ WSR - 303 NF TG LEO banner
IFF Pharma SolutionsPOLYOX™ WSR - 303 NF TG LEO
  • 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 - 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.
POLYOX™ WSR Coagulant FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant FP NF Grade
  • Chemical Name:Polyethylene Oxide, Pyrogenic Silica
  • 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, 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), 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 Coagulant FP 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 - N60K SFP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N60K SFP 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 - N60K SFP NF Grade an off-white powder, offers versatile applications. Its industrial additives function as binders and thickeners, aiding in direct compression manufacturing. In pharmaceuticals, it acts as a binder and controlled release agent. Soluble in water, it suits abuse deterrent tablets & capsules, gels, and osmotic pump tablets.
POLYOX™ WSR - N80 FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N80 FP 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 - N80 FP NF Grade with its off-white color and powder form, exhibits versatile applications. In cosmetics, it functions as both a binder and a thickener, while in industrial additives, it serves similar purposes, offering water solubility for ease of use across various formulations.
POLYOX™ WSR - 301 FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 301 FP 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 - 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.
ETHOCEL™ Medium 50 Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Medium 50 Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Controlled Release Agent, Granulation Aid, Binder, Taste Masker
  • Dosage Form:Tablets
  • Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Not Listed In California Proposition 65, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Ethylene Oxide-free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, Sewage Sludge Free, Plasticizer-free
  • Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), FDA 21 CFR 573.420, European Regulation 396/2005/EC, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, EC No. 1935/2004, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP
  • Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Encapsulation, Direct Compression
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.
POLYOX™ WSR - N750 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N750 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 - N750 NF Grade is available in various dosage forms including gels, osmotic pump tablets, and traditional tablets. Utilizing direct compression manufacturing technology, it serves applications in both oral and topical drug delivery within the healthcare and pharmaceutical markets. With its properties as a binder and thickener, this white, water-soluble powder aids in formulation processes.

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