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IFF Pharma Solutions

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32 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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POLYOX™ WSR - N12K LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K LEO 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N12K LEO 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.
METHOCEL™ E10M HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ E10M HPMC - Specialty
  • Functions:Green Strength Enhancer, Film Former, Controlled Release Agent, Anti-Settling Agent, Plasticizer, Binder, Surfactant, Lubricant (Internal), Rheology Modifier, Emulsifier, Rheology Modifier
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Dosage Form:Tablets
  • Certifications & Compliance:RoHS Compliant, RoHS 2 Compliant, Regulation (EU) No. 1830/2003, GMP, Regulation (EC) No. 1333/2008, Indian Pharmacopeia, Hazard Analysis Critical Control Point (HACCP), ISO 50001, Organic Certified, FDA 21 CFR 172.874, FDA 21 CFR 101.9, FDA 21 CFR 182.1480, FFDCA, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), cGMP, FDA Food Safety Modernization Act (FSMA), USDA Organic, 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, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Regulation (EU) No. 1829/2003, Regulation (EU) No. 10/2011 (PIM), Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, ISO 9001, Directive 1333/2008/EC, National Formulary (NF), Majelis Ulama Indonesia Halal, Orthodox Union Kosher, Regulation (EU) No. 1272/2008, FSSC 22000
  • Features:Wide pH Range, Cold Water Dispersible, Improved Dispersion, Improved Adhesion, High Cohesion, Low Surface Tension, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Good pH Stability, Anti-settling Properties, Low Ash Content, Thixotropic
METHOCEL™ E10M HPMC - Specialty derived from plants, acts as a rheology modifier. It meets high standards, being labeled as dioxin-free, dye-free, and hormone-free, ensuring its suitability for various industrial applications.
POLYOX™ WSR - N80 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N80 LEO 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N80 LEO 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.
Protanal® LF - 200M banner
IFF Pharma SolutionsProtanal® LF - 200M
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Endocrine Disruptor-free, Glycerin-free, Bactericide-free, NPE-free, Gold-Free, Plasticizer-free, Halal, PFOA-free, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Plant-Based, Tributyltin (TBT) - Free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Hormones-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Pesticide-free, Kosher, Solvent-free, Impurities-free, Antibiotics-free, Melamine-free, Barium-free, Naturally Derived, Cadmium-free, Colorants-free, Latex-free, Steroids Free, Potassium-free, Fungicide-free, Dioxin-free, Conflict minerals-free, Cobalt-free, Animal Products-free, GMO-free, Radioactive-free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Herbicide-free, Artificial Flavor-Free, Non-GMO, PAH-free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Quaternary Ammonium Salt-Free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Gluten-free, BSE-free, Irradiation-free, Sugar-free, Perfluorocarbon (PFC)-free, PVC-free, CMR Substances-free, Tin-free, No Artificial Sweeteners, Nanomaterials-free, Mycotoxins-free
  • Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), IFRA Compliant, Halal Food Council of Europe, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), Kosher, GMP, Clean Water Act (CWA) Certified, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 117, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), FFDCA
  • Chemical Inventories:IECSC (China), PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), ECL (Korea), DSL (Canada)
Protanal® LF- 200M is a versatile powder renowned for its role as a controlled release agent, gelling agent, thickener, stabilizer, and antacid in pharmaceutical and nutraceutical applications. Ensuring purity, it is swage-sludge-free, offering reliability in food ingredients.
POLYOX™ WSR - 301 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 301 LEO 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 301 LEO 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.
METHOCEL™ K15M HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ K15M HPMC - Specialty
  • Functions:Controlled Release Agent, Rheology Modifier
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Labeling Claims:Phthalates-free, Paraben-free, Aluminum-free, Nitrosamines-free, Preservative-free, Halal, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, Generally Recognized As Safe (GRAS), PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Dairy-free, VOC-free, TSE-free, Perfluorooctanoic Acid-free, Aflatoxin-free, Plant-Based, Endocrine Disruptor-free, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, Mycotoxins-free, Kosher, Bisphenol A-free, Dye Free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, APE-free, Pesticide-free, Triphenyl Tin Compounds-Free, CMR Substances-free, Plasticizer-free, Irradiation-free, Glycerin-free, 1,4-Dioxane-free, Sugar-free, Not Listed In California Proposition 65, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan
  • Certifications & Compliance:European Regulation 396/2005/EC, ISO 9001, RoHS 2 Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, FDA Food Safety Modernization Act (FSMA), EU Packaging Directive (94/62/EC), Regulation (EU) No. 10/2011 (PIM), Majelis Ulama Indonesia Halal, ISO 50001, Turkish RoHS Regulation, Swiss Ordinance (SR 817.023.21), Halal, Regulation (EU) No. 1830/2003, Directive 1333/2008/EC, USDA Organic, Doping-Free, Directive 2009/48/EC, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1829/2003, Chinese Pharmacopeia (ChP), FDA Compliant, ISO 14001, FSSC 22000, FDA 21 CFR 182.1480, JECFA (FAO/WHO), cGMP, European Pharmacopeia (Ph. Eur.), Clean Water Act (CWA) Certified, WEEE Directive 2012/19/EU, Regulation (EU) No. 2022/1396, Organic Certified, Directive 2023/915/EU, Orthodox Union Kosher, Regulation (EU) No. 231/2012, RoHS Compliant, FEMA Compliant, FDA 21 CFR 101.9, Clean Air Act (CAA) Certified, FDA 21 CFR 172.874, Regulation (EU) No. 1272/2008, Kosher, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant
  • Dosage Form:Tablets
METHOCEL™ K15M HPMC - Specialty known for its water solubility and derived from hypromellose, acts as a rheology modifier. It's noteworthy for its labeling claims, including being free from parabens, perfluorooctanoic acid (PFOA), pesticides, and per- and polyfluoroalkyl substances (PFAS).
ETHOCEL™ Standard 20 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 20 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:Caffeine Free, Organic, Irradiation-free, VOC-free, Quaternary Ammonium Salt-Free, PFOS-free, Dioxane-free, Dairy-free, Odor-free, Tributyltin (TBT) - Free, Allergen-free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Zero Calorie, Nitrosamines-free, Bisphenol Derivatives-free, Pesticide-free, Non-GMO, Kosher, Hormones-free, APE-free, Sugar-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, FSSC 22000, PHO (Partially Hydrogenated Oil)-Free, Iodide-free, Gluten-free, Sewage Sludge Free, Paraben-free, Phthalates-free, Dye Free, 1,4-Dioxane-free, PAH-free, Halal, Preservative-free, PVC-free, PFOA-free, Potassium-free, Aluminum-free, PFAS-Free, Antibiotics-free, Non-Irritant, Non-Mutagenic
  • Color (Properties):White
  • Certifications & Compliance:FDA 21 CFR 101.9, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, ISO 9001, Organic Certified, cGMP, GMP, Directive 1333/2008/EC, ICH Q3C, Directive 2011/65/EU (RoHS 2), FSSC 22000, United States Pharmacopeia (USP), EFSA (European Food Safety Authority) Certified, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 172.868, FSC Certified, JECFA (FAO/WHO), FDA Food Safety Modernization Act (FSMA), RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), EuPIA Listed, Regulation (EU) No. 10/2011 (PIM), Regulation (EC) No. 1333/2008, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Regulation (EU) No. 1272/2008, Directive 2012/19/EU, Directive 2009/48/EC, Halal, USDA Organic, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), Kosher, FDA 21 CFR 117, Chinese Pharmacopeia (ChP), Clean Water Act (CWA) Certified
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 20 Industrial Ethylcellulose - Specialty is tailored for spray and phenolics applications, featuring good printability, reduced tack, and scuff resistance. Acting as a stabilizer, it is available in powder or granule form, ensuring compatibility with organic solvents and offering a white color for versatility in industrial processes.
POLYOX™ WSR - N60K LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N60K LEO NF Grade
  • Chemical Name:Polyethylene Oxide, Pyrogenic Silica
  • 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, 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N60K LEO 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 - 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, 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.
METHOCEL™ 228S HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ 228S HPMC - Specialty
  • Functions:Green Strength Enhancer, Film Former, Controlled Release Agent, Anti-Settling Agent, Plasticizer, Binder, Surfactant, Lubricant (Internal), Rheology Modifier, Emulsifier, Rheology Modifier
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Dosage Form:Tablets
  • Certifications & Compliance:RoHS Compliant, RoHS 2 Compliant, Regulation (EU) No. 1830/2003, GMP, Regulation (EC) No. 1333/2008, Indian Pharmacopeia, Hazard Analysis Critical Control Point (HACCP), ISO 50001, Organic Certified, FDA 21 CFR 172.874, FDA 21 CFR 101.9, FDA 21 CFR 182.1480, FFDCA, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), FCC Compliant, cGMP, FDA Food Safety Modernization Act (FSMA), USDA Organic, EU Directive 2002/72/EC, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, EC No. 1935/2004, EU Cosmetic Regulation 1223/2009 Compliant, British Pharmacopeia (BP), Doping-Free, Turkish RoHS Regulation, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, EC No. 2023/2006, Regulation (EU) No. 1829/2003, Regulation (EU) No. 10/2011 (PIM), Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, ISO 9001, Directive 1333/2008/EC, National Formulary (NF), Majelis Ulama Indonesia Halal, Orthodox Union Kosher, Regulation (EU) No. 1272/2008, FSSC 22000
  • Features:Wide pH Range, Cold Water Dispersible, Improved Dispersion, Improved Adhesion, High Cohesion, Low Surface Tension, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Good pH Stability, Anti-settling Properties, Low Ash Content, Thixotropic
METHOCEL™ 228S HPMC - Specialty is a versatile pharmaceutical and nutraceutical excipient used in various dosage forms, including tablets, capsules, and suspensions. It is applied in manufacturing technologies such as tablet coating, granulation, and wet granulation. METHOCEL™ Specialty 228S HPMC functions as a controlled release agent, immediate release agent, thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive. It is water-soluble, making it an excellent choice for a range of applications.
ETHOCEL™ Standard 100 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 100 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:Caffeine Free, Organic, Irradiation-free, VOC-free, Quaternary Ammonium Salt-Free, PFOS-free, Dioxane-free, Dairy-free, Odor-free, Tributyltin (TBT) - Free, Allergen-free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Zero Calorie, Nitrosamines-free, Bisphenol Derivatives-free, Pesticide-free, Non-GMO, Kosher, Hormones-free, APE-free, Sugar-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, FSSC 22000, PHO (Partially Hydrogenated Oil)-Free, Iodide-free, Gluten-free, Sewage Sludge Free, Paraben-free, Phthalates-free, Dye Free, 1,4-Dioxane-free, PAH-free, Halal, Preservative-free, PVC-free, PFOA-free, Potassium-free, Aluminum-free, PFAS-Free, Antibiotics-free, Non-Irritant, Non-Mutagenic
  • Color (Properties):White
  • Certifications & Compliance:FDA 21 CFR 101.9, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, ISO 9001, Organic Certified, cGMP, GMP, Directive 1333/2008/EC, ICH Q3C, Directive 2011/65/EU (RoHS 2), FSSC 22000, United States Pharmacopeia (USP), EFSA (European Food Safety Authority) Certified, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 172.868, FSC Certified, JECFA (FAO/WHO), FDA Food Safety Modernization Act (FSMA), RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), EuPIA Listed, Regulation (EU) No. 10/2011 (PIM), Regulation (EC) No. 1333/2008, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Regulation (EU) No. 1272/2008, Directive 2012/19/EU, Directive 2009/48/EC, Halal, USDA Organic, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), Kosher, FDA 21 CFR 117, Chinese Pharmacopeia (ChP), Clean Water Act (CWA) Certified
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 100 Industrial Ethylcellulose - Specialty is a versatile choice for spray and phenolics applications. It functions as a thickener, rheology modifier, binder & resin, and film former. Available in powder or granule form, its white color ensures compatibility with various industrial needs.
ETHOCEL™ Standard 14 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 14 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:Caffeine Free, Organic, Irradiation-free, VOC-free, Quaternary Ammonium Salt-Free, PFOS-free, Dioxane-free, Dairy-free, Odor-free, Tributyltin (TBT) - Free, Allergen-free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Zero Calorie, Nitrosamines-free, Bisphenol Derivatives-free, Pesticide-free, Non-GMO, Kosher, Hormones-free, APE-free, Sugar-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, FSSC 22000, PHO (Partially Hydrogenated Oil)-Free, Iodide-free, Gluten-free, Sewage Sludge Free, Paraben-free, Phthalates-free, Dye Free, 1,4-Dioxane-free, PAH-free, Halal, Preservative-free, PVC-free, PFOA-free, Potassium-free, Aluminum-free, PFAS-Free, Antibiotics-free, Non-Irritant, Non-Mutagenic
  • Color (Properties):White
  • Certifications & Compliance:EU Directive 2002/72/EC, FDA 21 CFR 101.9, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, ISO 9001, Organic Certified, cGMP, GMP, Directive 1333/2008/EC, ICH Q3C, EC No. 2023/2006, Directive 2011/65/EU (RoHS 2), FSSC 22000, United States Pharmacopeia (USP), EFSA (European Food Safety Authority) Certified, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 172.868, FSC Certified, JECFA (FAO/WHO), FDA Food Safety Modernization Act (FSMA), RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), EuPIA Listed, Regulation (EU) No. 10/2011 (PIM), Regulation (EC) No. 1333/2008, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Regulation (EU) No. 1272/2008, Directive 2012/19/EU, Directive 2009/48/EC, Halal, USDA Organic, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), EC No. 1935/2004, Kosher, FDA 21 CFR 117, Chinese Pharmacopeia (ChP), Clean Water Act (CWA) Certified
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 14 Industrial Ethylcellulose - Specialty is perfect for spray and phenolics applications. Available in powder or granule forms, its white color ensures versatility. Acting as a thickener, rheology modifier, and binder & resin, it guarantees consistent performance in various industrial settings.
METHOCEL™ K100 LV HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ K100 LV HPMC - Specialty
  • Functions:Controlled Release Agent, Rheology Modifier
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Labeling Claims:Phthalates-free, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Allergen-free, Halal, Potassium-free, PAH-free, Caffeine Free, Sewage Sludge Free, Herbicide-free, PFOA-free, Diethylene Glycol-free, Gluten-free, PHO (Partially Hydrogenated Oil)-Free, Persistent Organic Pollutants (POP)-free, Monosodium Glutamate (MSG)-free, Dairy-free, VOC-free, TSE-free, Aflatoxin-free, Endocrine Disruptor-free, Quaternary Ammonium Salt-Free, Iodide-free, Latex-free, Vegetarian, Non-GMO, Palm Oil-free, Ethylene Glycol-free, Mycotoxins-free, Kosher, Dye Free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Organic, Tributyltin (TBT) - Free, APE-free, Pesticide-free, Bisphenol Derivatives-free, CMR Substances-free, Dioxane-free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, Not Listed In California Proposition 65, PFOS-free, Fungicide-free, BSE-free, Natural Latex Rubber-Free, Vegan
  • Certifications & Compliance:ISO 9001, Generally Recognized As Safe (GRAS), United States Pharmacopeia (USP), Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 10/2011 (PIM), ISO 50001, FDA 21 CFR 175.300, Turkish RoHS Regulation, Swiss Ordinance (SR 817.023.21), Halal, Regulation (EU) No. 1830/2003, Directive 1333/2008/EC, USDA Organic, Directive 2009/48/EC, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1829/2003, Chinese Pharmacopeia (ChP), FDA Compliant, FDA 21 CFR 175.105, ISO 14001, FSSC 22000, Nagoya Compliant, FDA 21 CFR 176.180, cGMP, European Pharmacopeia (Ph. Eur.), ICH Q3C, Clean Water Act (CWA) Certified, Regulation (EU) No. 2022/1396, FDA 21 CFR 174.5, Organic Certified, FSC Certified, Orthodox Union Kosher, Waste Electrical & Electronic Equipment Directive (WEEE), Regulation (EU) No. 231/2012, FDA 21 CFR 101.9, FDA 21 CFR 172.874, Regulation (EU) No. 1272/2008, Indian Pharmacopeia, Kosher, EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170
  • Dosage Form:Tablets
METHOCEL™ K100 LV HPMC - Specialty known as both cellulose ethers and hypromellose, serves as a rheology modifier, ensuring consistency in formulations. Notably, it is water-soluble, making it suitable for various applications.
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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, 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.
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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, 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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