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IFF Pharma Solutions

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132 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.
METHOCEL™ 10-0352 Cellulose Ether - Specialty banner
IFF Pharma SolutionsMETHOCEL™ 10-0352 Cellulose Ether - Specialty
  • INCI Name:Methylcellulose, Hydroxypropyl Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Dosage Form:Tablets
  • Labeling Claims:Phthalates-free, Steroids Free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, Radioactive-free, Potassium-free, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, Artificial Flavor-Free, Herbicide-free, NPE-free, PFOA-free, Diethylene Glycol-free, Gluten-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Dairy-free, VOC-free, TSE-free, Pareve, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Quaternary Ammonium Salt-Free, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, Ethylene Glycol-free, Mycotoxins-free, Kosher, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, Tributyltin (TBT) - Free, Bactericide-free, No Artificial Sweeteners, APE-free, Pesticide-free, CMR Substances-free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, PFOS-free, Fungicide-free, Perfluorocarbon (PFC)-free, BSE-free, Natural Latex Rubber-Free, Impurities-free, Vegan, Low Odor
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.
POLYOX™ WSR - N12K FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K 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, Kosher, Vegan, TSE-free, Diethylene Glycol-free, Fungicide-free, Pesticide-free, Allergen-free, Residual Solvent -Free, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, Herbicide-free, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free, Gluten-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, EC No. 1935/2004, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, 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), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, FFDCA, 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
POLYOX™ WSR - N12K FP NF Grade composed of ethylene oxide copolymers and polyethylene oxide, serves diverse functions in pharmaceutical formulations. It finds application in abuse-deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. This versatile ingredient acts as a binder, thickener, and controlled release agent, ensuring optimal performance. Available in powder form, it demonstrates water solubility, facilitating easy integration into formulations for enhanced effectiveness.
POLYOX™ N60K LEO NF HV banner
IFF Pharma SolutionsPOLYOX™ N60K LEO NF HV
  • Chemical Name:Polyethylene Oxide, Polyethylene Glycol, 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, Kosher, Vegan, TSE-free, Diethylene Glycol-free, Fungicide-free, Pesticide-free, Allergen-free, Residual Solvent -Free, Ethylene Glycol-free, Oxidatively Degradable, Irradiation-free, Animal Products-free, Dairy-free, Not Tested on Animals, Ethylene Oxide-free, Herbicide-free, Doping Substances-free, VOC-free, BSE-free, Halal, Non-GMO, Zinc-free, Gluten-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, EC No. 1935/2004, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, 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), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, FFDCA, 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
POLYOX™ N60K LEO NF HV containing polyethylene oxide (PEG-45M) serves multiple functions in various applications. Its versatility extends to deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. Functioning as a thickener, binder, and controlled release agent, it ensures optimal formulation performance. Available in powder form, it exhibits water solubility, enhancing its usability in diverse pharmaceutical formulations.
Protanal® AR - 1410 banner
IFF Pharma SolutionsProtanal® AR - 1410
  • Chemical Name:Sodium Alginate
  • Labeling Claims: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, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Impurities-free, Antibiotics-free, Melamine-free, Barium-free, Cadmium-free, Naturally Derived, Colorants-free, Steroids Free, Latex-free, Potassium-free, Fungicide-free, Conflict minerals-free, Dioxin-free, Cobalt-free, Animal Products-free, GMO-free, Radioactive-free, Natural Latex Rubber-Free, 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, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, Perfluorocarbon (PFC)-free, PVC-free, CMR Substances-free, No Artificial Sweeteners, Tin-free, Nanomaterials-free, Mycotoxins-free, Endocrine Disruptor-free, Glycerin-free, Bactericide-free
  • Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, IFRA Compliant, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), Kosher, GMP, 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
Protanal® AR - 1410 is a versatile powder designed for various functions in the pharmaceutical and nutraceutical industries. It serves as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid, ensuring optimal performance in formulations. Crafted to be sewage sludge-free, it meets high standards of quality and safety.
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.
Protanal® LF - 120LS banner
IFF Pharma SolutionsProtanal® LF - 120LS
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Halal, Paraben-free, Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free
  • Certifications & Compliance:Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, 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, FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP)
  • Chemical Inventories:PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China)
Protanal® LF - 120LS proudly boasts its labeling claims, ensuring it is free from glycerin, endocrine disruptors, cadmium, and suitable for vegetarians. This versatile powder serves various functions in pharmaceuticals, functioning as both emulsifiers, stabilizers, and aiding in modified and controlled release formulations.
POLYOX™ WSR - 205 FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 205 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, Kosher, Vegan, TSE-free, Diethylene Glycol-free, Fungicide-free, Pesticide-free, Allergen-free, Residual Solvent -Free, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, Herbicide-free, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free, Gluten-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, EC No. 1935/2004, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, 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), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, FFDCA, 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
POLYOX™ WSR - 205 FP NF Grade comprising ethylene oxide copolymers and polyethylene oxide (PEG-14M), serves multiple functions across various pharmaceutical applications. Its versatility extends to deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. Functioning as a binder and thickener, it ensures optimal formulation performance. Available in powder form, it exhibits water solubility, facilitating ease of use in pharmaceutical formulations.

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