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165 Products found on IFF Pharma Solutions

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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.
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.
ETHOCEL™ Standard 4 Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 4 Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
  • Dosage Form:Tablets
  • Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Dye Free, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, GMO-free, Sewage Sludge Free, Plasticizer-free
  • Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), European Regulation 396/2005/EC, FDA 21 CFR 573.420, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Halal, Directive 2023/915/EU, Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, Kosher, ICH Q3C, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
  • Manufacturing Technology:Hot Melt Extrusion, Encapsulation, Direct Compression, Granulation, Tablet Coating
ETHOCEL™ Standard 4 Premium Ethylcellulose is a white powder that is soluble in ethanol and organic solvents. It provides benefits such as binding, controlled release, excellent flexibility, and thermal stability, making it highly suitable for various industrial applications where these properties are critical.
Manucol® DH banner
IFF Pharma SolutionsManucol® DH
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-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, Odor-free, Palm Oil-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free, Halal, Paraben-free
  • Certifications & Compliance:IFRA Compliant, Halal Food Council of Europe, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Chinese Pharmacopeia (ChP), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008
  • Chemical Inventories:KECI (Korea), PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), DSL (Canada), IECSC (China)
Manucol® DH cobalt, barium, and gold-free, functions as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, serving diverse roles in pharmaceutical and nutraceutical applications.
METHOCEL™ E4M Premium CR HPMC banner
IFF Pharma SolutionsMETHOCEL™ E4M Premium CR HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Sustained Release Agent, Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Mucoadhesive, Viscosity Modifier, Binder, Gelling Agent, Plasticizer, Controlled Release Agent, Film Former, Thickener, Immediate Release Agent, Solubilizer
  • Dosage Form:Tablets, Suspension
  • Labeling Claims:Kosher, Vegan, Zero Calorie, Colorants-free, Hypoallergenic, Pesticide-free, Allergen-free, PAH-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, USP 232 Elemental Impurities Free, 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, Animal Products-free, Monosodium Glutamate (MSG)-free, Odor-free, Perfluorooctanoic Acid-free, Palm Oil-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), Hazard Analysis Critical Control Point (HACCP), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Directive 1333/2008/EC, Regulation (EC) No. 1333/2008, Orthodox Union Kosher, Organic Certified, FDA 21 CFR 172.874, ISO 14001, Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), National Formulary (NF), EXCiPACT, USDA Organic, Regulation (EU) No. 1829/2003, Directive 2009/48/EC, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, European Regulation 396/2005/EC, FDA Compliant, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), FDA 21 CFR 182.1480, cGMP, CFDA Compliant (China), ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, FCC Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Granulation, Tablet Coating
METHOCEL™ E4M Premium CR HPMC is water-soluble and used in suspensions, granulation, and tablet coating. It serves as a binder, controlled release agent, film former, gelling agent, and immediate release agent in pharmaceuticals and nutraceuticals, and as a binder in ceramics.
METHOCEL™ A4C Premium Methylcellulose banner
IFF Pharma SolutionsMETHOCEL™ A4C Premium Methylcellulose
  • Chemical Name:Methylcellulose
  • CAS Number:9004-67-5
  • Functions:Controlled Release Agent, Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Film Former, Thickener, Mucoadhesive, Suspending Agent, Viscosity Modifier, Binder, Gelling Agent, Solubilizer, Plasticizer
  • Dosage Form:Tablets
  • Labeling Claims:Antibiotics-free, Pareve, Gluten-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Dye Free, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Allergen-free, PAH-free, Plant-Based, Irradiation-free, Animal Products-free, USP 232 Elemental Impurities Free, Melamine-free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, APE-free, Tributyl Tin Compounds-Free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Japan Pharmacopeia (JP), FDA 21 CFR 101.9, European Regulation 396/2005/EC, FSSC 22000, USDA Certified, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, United States Pharmacopeia (USP), Organic Certified, FDA 21 CFR 172.874, ISO 14001, EC No.1907/2006, Indian Pharmacopeia, FDA 21 CFR 182.1480, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, National Formulary (NF), FCC Compliant, EXCiPACT, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
  • Manufacturing Technology:Granulation, Tablet Coating
METHOCEL™ A4C Premium Methylcellulose manufactured using granulation technology, serves various functions in pharmaceutical and nutraceutical applications. It acts as a binder, film former, gelling agent, mucoadhesive, thickener, and viscosity modifier, ensuring optimal performance and formulation versatility.
Protanal® LF - 10/60FT banner
IFF Pharma SolutionsProtanal® LF - 10/60FT
  • Chemical Name:Sodium Alginate
  • Labeling Claims: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, 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, Halal, Paraben-free
  • Certifications & Compliance:IFRA Compliant, Halal Food Council of Europe, 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), Regulation (EU) No. 1272/2008
  • Chemical Inventories:PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China)
Protanal® LF - 10/60FT composed of sodium alginate, originates from non-animal sources. It serves various functions in pharmaceuticals and nutraceuticals, including as an antacid, controlled release agent, gelling agent, and thickener, available in powder form.
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 - 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 - 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.
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.
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 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.
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), 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 - 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.
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.

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