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IFF Pharma Solutions

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55 Products found on IFF Pharma Solutions

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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), 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 - 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 Coagulant NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
  • Dosage Form:Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
  • Labeling Claims:Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR Coagulant NF Grade is an off-white, water-soluble powder used in pharmaceutical and nutraceutical applications for direct compression manufacturing, functioning as a binder and controlled release agent.
ETHOCEL™ Standard 10 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 10 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose Ethers, Cellulose & Cellulosics
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:FSSC 22000, Not Listed In California Proposition 65, Sugar-free, Iodide-free, 1,4-Dioxane-free, Nitrosamines-free, Gluten-free, Quaternary Ammonium Salt-Free, Plasticizer-free, Halal, PFOS-free, Bisphenol Derivatives-free, Caffeine Free, Irradiation-free, Odor-free, VOC-free, PFAS-Free, Kosher, Tributyltin (TBT) - Free, PAH-free, Natural Latex Rubber-Free, Organic, Allergen-free, Dioxane-free, Antibiotics-free, Hormones-free, Dairy-free, Zero Calorie, Monosodium Glutamate (MSG)-free, Phthalates-free, Paraben-free, Non-Mutagenic, Non-Irritant, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, Aluminum-free, Sewage Sludge Free, Potassium-free, PFOA-free, PVC-free, Pesticide-free
  • Color (Properties):White
  • Certifications & Compliance:Chinese Pharmacopeia (ChP), Clean Water Act (CWA) Certified, ICH Q3C, EFSA (European Food Safety Authority) Certified, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, Kosher, ISO 9001, Organic Certified, Regulation (EU) No. 10/2011 (PIM), GMP, Directive 1333/2008/EC, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 117, FSSC 22000, United States Pharmacopeia (USP), FDA Compliant, EuPIA Listed, Regulation (EU) No. 231/2012, USDA Organic, Regulation (EC) No. 1333/2008, FSC Certified, JECFA (FAO/WHO), cGMP, FDA 21 CFR 172.868, RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Directive 2012/19/EU, Regulation (EU) No. 1272/2008, Directive 2009/48/EC, Halal, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), FDA 21 CFR 101.9
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 10 Industrial Ethylcellulose - Specialty is tailored for modified rosins, alkyds (Long Oil), and phenolics. With benefits like being aluminum-free, antibiotics-free, APE-free, bisphenol derivatives-free, caffeine-free, and dioxane-free, it ensures product purity and safety. Notable features include scuff resistance, serving as a stabilizer, thickener, rheology modifier, binder & resin, and film former, guaranteeing optimal performance in various industrial applications.
SeaGel® CAP - 201 banner
IFF Pharma SolutionsSeaGel® CAP - 201
  • Chemical Name:Carrageenan
  • Functions:Encapsulant, Controlled Release Agent
  • Labeling Claims:Organic, Paraben-free, PFOA-free, Phthalates-free, Non-GMO, Not Listed In California Proposition 65, Fungicide-free, Dye Free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Environmentally Friendly, Natural, Plant-Based, Iodide-free, Aluminum-free, PAH-free, TSE-free, Sustainable, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Bisphenol Derivatives-free, Herbicide-free, Palm Oil-free, APE-free, Clean Label, Tributyltin (TBT) - Free, Preservative-free, Kosher, Sugar-free, Hormones-free, Potassium-free, Naturally Derived, PFAS-Free, Quaternary Ammonium Salt-Free, Vegetarian, Nitrosamines-free, Antibiotics-free, Doping Substances-free, Animal Products-free, Plasticizer-free, Dioxane-free, Allergen-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free, Gluten-free
  • Certifications & Compliance:Directive 1333/2008/EC, Regulation (EU) No. 1829/2003, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, FSSC 22000, ISO 9001, cGMP, Regulation (EU) No. 1272/2008, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Directive 396/2005/EC, FDA 21 CFR 177.1520, Clean Water Act (CWA) Certified, Nagoya Compliant, Orthodox Union Kosher, FDA 21 CFR 179.26
  • Dosage Form:Capsules
SeaGel® CAP - 201 identified as carrageenan, offers versatility and quality in capsule applications. With its natural and non-animal plant origins, it ensures ethical sourcing. Featuring easy-to-use powder form, it boasts film-forming properties, heat, and thermal stability. Additionally, it functions as an encapsulant and controlled release agent, providing enhanced performance in encapsulation processes.
METHOCEL™ 240 HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ 240 HPMC - Specialty
  • Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal)
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Dosage Form:Tablets
  • Certifications & Compliance:Clean Water Act (CWA) Certified, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS), RoHS Compliant, RoHS 2 Compliant, Regulation (EC) No. 1333/2008, cGMP, Majelis Ulama Indonesia Halal, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), ISO 50001, Organic Certified, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), USDA Organic, FDA 21 CFR 182.1480, FFDCA, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), European Regulation 396/2005/EC, EU Cosmetic Regulation 1223/2009 Compliant, Doping-Free, Clean Air Act (CAA) Certified, Turkish RoHS Regulation, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008
  • Features:Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range, Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties
METHOCEL™ 240 HPMC - Specialty sourced from plants, is recognized for its aluminum, antibiotics, APE, bisphenol A, and caffeine-free composition. It functions as a rheology modifier in industrial additives.
ETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose Ethers, Cellulose & Cellulosics
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:FSSC 22000, Not Listed In California Proposition 65, Sugar-free, Iodide-free, 1,4-Dioxane-free, Nitrosamines-free, Gluten-free, Quaternary Ammonium Salt-Free, Plasticizer-free, Halal, PFOS-free, Bisphenol Derivatives-free, Caffeine Free, Irradiation-free, Odor-free, VOC-free, PFAS-Free, Kosher, Tributyltin (TBT) - Free, PAH-free, Natural Latex Rubber-Free, Organic, Allergen-free, Dioxane-free, Antibiotics-free, Hormones-free, Dairy-free, Zero Calorie, Monosodium Glutamate (MSG)-free, Phthalates-free, Paraben-free, Non-Mutagenic, Non-Irritant, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, Aluminum-free, Sewage Sludge Free, Potassium-free, PFOA-free, PVC-free, Pesticide-free
  • Color (Properties):White
  • Certifications & Compliance:Chinese Pharmacopeia (ChP), Clean Water Act (CWA) Certified, ICH Q3C, EFSA (European Food Safety Authority) Certified, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, Kosher, ISO 9001, Organic Certified, Regulation (EU) No. 10/2011 (PIM), GMP, Directive 1333/2008/EC, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 117, FSSC 22000, United States Pharmacopeia (USP), FDA Compliant, EuPIA Listed, Regulation (EU) No. 231/2012, USDA Organic, Regulation (EC) No. 1333/2008, FSC Certified, JECFA (FAO/WHO), cGMP, FDA 21 CFR 172.868, RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Directive 2012/19/EU, Regulation (EU) No. 1272/2008, Directive 2009/48/EC, Halal, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), FDA 21 CFR 101.9
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty is optimized for spray, phenolics, and modified rosins applications. It features good printability, reduced tack, and scuff resistance, ensuring high-quality finishes. Serving as a stabilizer and thickener, it is available in both powder and granule forms, presenting a white color for versatility in industrial processes.
POLYOX™ WSR - N750 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N750 LEO NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
  • Dosage Form:Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
  • Labeling Claims:Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N750 LEO 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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