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IFF Pharma Solutions

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42 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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POLYOX™ WSR - 1105 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 1105 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, 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, 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 - 1105 LEO NF Grade an off-white powder, serves as a binder and thickener in cleaning agents. It is available in powder form and is water-soluble, making it suitable for use in gels and osmotic pump tablets.
POLYOX™ WSR - N60K NF banner
IFF Pharma SolutionsPOLYOX™ WSR - N60K NF
  • 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, 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 NF 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 - 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, 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 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™ K4M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ K4M Modified Cellulose Food Grade - Specialty
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Functions:Controlled Release Agent
  • Labeling Claims:Endocrine Disruptor-free, Glycerin-free, Perfluorooctanoic Acid-free, Hypoallergenic, Triphenyl Tin Compounds-Free, Plasticizer-free, Dairy-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Plant-Based, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Sewage Sludge Free, PFOS-free, Nitrosamines-free, Hormones-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Pesticide-free, Kosher, Antibiotics-free, Naturally Derived, Colorants-free, Dioxin-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Low Odor, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Bisphenol A-free, Generally Recognized As Safe (GRAS), Zero Calorie, APE-free, BSE-free, Irradiation-free, Organic, Sugar-free, PVC-free, Dye Free, CMR Substances-free, VOC-free, Mycotoxins-free
  • Certifications & Compliance:FSSC 22000, cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, FDA 21 CFR 176.180, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), FDA 21 CFR 175.105, USDA Organic, Swiss Ordinance (SR 817.023.21), ICH Q3C, FDA 21 CFR 101.9, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, FDA 21 CFR 172.874, FDA 21 CFR 182.1480, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, Regulation (EU) No. 1829/2003, GMP, FEMA Compliant, Halal, Doping-Free, ISO 14001, National Formulary (NF), Regulation (EC) No. 1333/2008, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, Regulation (EU) No. 1830/2003, Directive 2023/2055/EU, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1935/2004, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FDA 21 CFR 174.5, FDA 21 CFR 175.300, Organic Certified, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, Orthodox Union Kosher, EU Packaging Directive (94/62/EC)
  • Dosage Form:Tablets
METHOCEL™ K4M Modified Cellulose Food Grade - Specialty a food-grade product, acts as a binder, controlled release agent, film former, and gelling agent in pharmaceuticals and nutraceuticals. It facilitates granulation and tablet coating processes and exhibits water solubility.
METHOCEL™ F50 Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ F50 Modified Cellulose Food Grade - Specialty
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Functions:Controlled Release Agent
  • Labeling Claims:Endocrine Disruptor-free, Glycerin-free, Perfluorooctanoic Acid-free, Hypoallergenic, Triphenyl Tin Compounds-Free, Plasticizer-free, Dairy-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Plant-Based, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Sewage Sludge Free, PFOS-free, Nitrosamines-free, Hormones-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Pesticide-free, Kosher, Antibiotics-free, Naturally Derived, Colorants-free, Dioxin-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Low Odor, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Bisphenol A-free, Generally Recognized As Safe (GRAS), Zero Calorie, APE-free, BSE-free, Irradiation-free, Organic, Sugar-free, PVC-free, Dye Free, CMR Substances-free, VOC-free, Mycotoxins-free
  • Certifications & Compliance:FSSC 22000, cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, FDA 21 CFR 176.180, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), FDA 21 CFR 175.105, USDA Organic, Swiss Ordinance (SR 817.023.21), ICH Q3C, FDA 21 CFR 101.9, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, FDA 21 CFR 172.874, FDA 21 CFR 182.1480, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, Regulation (EU) No. 1829/2003, GMP, FEMA Compliant, Halal, Doping-Free, ISO 14001, National Formulary (NF), Regulation (EC) No. 1333/2008, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, REACH Exempt (Europe), ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, Regulation (EU) No. 1830/2003, Directive 2023/2055/EU, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1935/2004, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FDA 21 CFR 174.5, FDA 21 CFR 175.300, Organic Certified, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, Orthodox Union Kosher, EU Packaging Directive (94/62/EC)
  • Dosage Form:Tablets
METHOCEL™ F50 Modified Cellulose Food Grade - Specialty a modified cellulose of food grade, contains hypromellose and is manufactured using granulation and tablet coating technologies. It serves various functions in pharmaceuticals and nutraceuticals, including film formation, gelling, immediate and sustained release, as well as mucoadhesion and viscosity modification, thanks to its water-soluble nature.
POLYOX™ WSR - N10 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N10 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, 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, 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 - N10 LEO NF Grade an off-white powder, is prized for its water solubility, making it an effective binder and thickener in both cleaning and cosmetic products. Its versatility and solubility make it a valuable ingredient for various formulations.
METHOCEL™ E4M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ E4M Modified Cellulose Food Grade - Specialty
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Functions:Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Binder, Plasticizer, Controlled Release Agent
  • Labeling Claims:Monosodium Glutamate (MSG)-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Pesticide-free, Antibiotics-free, Naturally Derived, Colorants-free, Dioxin-free, Animal Products-free, Low Odor, Non-GMO, Tributyl Tin Compounds-Free, Odor-free, Pareve, Bisphenol A-free, Organic, Sugar-free, PVC-free, Dye Free, CMR Substances-free, Endocrine Disruptor-free, Glycerin-free, Perfluorooctanoic Acid-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Dairy-free, Halal, Paraben-free, Allergen-free, Aflatoxin-free, Sewage Sludge Free, PFOS-free, Vegan, Caffeine Free, Kosher, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, PAH-free, TSE-free, Palm Oil-free, Vegetarian, Zero Calorie, APE-free, BSE-free, Irradiation-free, VOC-free, Mycotoxins-free, Hypoallergenic, Aluminum-free, Preservative-free, Plant-Based
  • Certifications & Compliance:FDA 21 CFR 176.180, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), USDA Organic, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, EC No. 2023/2006, GMP, Halal, Doping-Free, Regulation (EC) No. 1333/2008, ISO 9001, Directive 2023/2055/EU, Regulation (EU) No. 10/2011 (PIM), EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 174.5, FDA 21 CFR 175.300, Organic Certified, Directive 2009/48/EC, Orthodox Union Kosher, EU Packaging Directive (94/62/EC), FFDCA, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008, FDA 21 CFR 175.105, ICH Q3C, FDA 21 CFR 101.9, FDA 21 CFR 172.874, FDA 21 CFR 182.1480, JECFA (FAO/WHO), Regulation (EU) No. 1829/2003, ISO 14001, National Formulary (NF), Indian Pharmacopeia, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, FDA 21 CFR 176.170, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), FCC Compliant, British Pharmacopeia (BP), cGMP, Regulation (EU) No. 1169/2011
  • Dosage Form:Tablets
METHOCEL™ E4M Modified Cellulose Food Grade - Specialty is water-soluble and used in granulation and tablet coating manufacturing. It functions as a binder, controlled release agent, film former, gelling agent, immediate release agent, mucoadhesive, and solubilizer in pharmaceuticals and nutraceuticals.
POLYOX™ WSR Coagulant LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant 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, 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, 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 Coagulant LEO 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.
METHOCEL™ F4M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ F4M Modified Cellulose Food Grade - Specialty
  • Ingredient Name:Hydroxypropyl Methyl Cellulose (HPMC)
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Ingredient Origin:Plant Origin
  • Functions:Controlled Release Agent, Film Former, Viscosity Modifier, Binder, Thickener
  • Labeling Claims:Kosher, Vegan, Zero Calorie, Colorants-free, Hypoallergenic, Pesticide-free, Generally Recognized As Safe (GRAS), PAH-free, Plant-Based, Phthalates-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, PFOS-free, VOC-free, BSE-free, Organic, Antibiotics-free, Pareve, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Naturally Derived, TSE-free, PVC-free, Aluminum-free, Glycerin-free, Sugar-free, Irradiation-free, Monosodium Glutamate (MSG)-free, Odor-free, Dairy-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, Paraben-free, Halal, Non-GMO, Low Odor, Sewage Sludge Free, Plasticizer-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Swiss Ordinance (SR 817.023.21), JECFA (FAO/WHO), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, Directive 1333/2008/EC, Regulation (EC) No. 1333/2008, Orthodox Union Kosher, Regulation (EU) No. 1935/2004, Organic Certified, FDA 21 CFR 172.874, 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, FEMA Compliant, European Regulation 396/2005/EC, FDA Compliant, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), FDA 21 CFR 176.180, FDA 21 CFR 182.1480, cGMP, Kosher, ICH Q3C, Regulation (EU) No. 1169/2011, EC No. 2023/2006, FCC Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 2022/1396, Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), REACH Exempt (Europe), Directive 2023/2055/EU, Regulation (EU) No. 1830/2003
  • Physical Form:Powder
  • Dosage Form:Tablets
METHOCEL™ F4M Modified Cellulose Food Grade - Specialty known for its water solubility, is utilized in various pharmaceutical and nutraceutical applications. It serves as a controlled release agent, film former, and gelling agent. Its manufacturing involves granulation and tablet coating processes.
POLYOX™ WSR - 303 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 303 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 - 303 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 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 303 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, 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, 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 - 303 LEO 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 Coagulant NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant 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 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.
POLYOX™ WSR - 301 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 301 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, 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, 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 NF Grade containing polyethylene oxide, is off-white in color and serves as a binder and thickener in both cosmetic and industrial applications. Additionally, it functions as a binder and controlled release agent in pharmaceuticals and nutraceuticals. It is available in powder form.

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