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201 Products found on IFF Pharma Solutions

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METHOCEL™ 240S HPMC - Specialty banner
IFF Pharma SolutionsMETHOCEL™ 240S HPMC - 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, Ozone Non Depleting, 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, 1,4-Dioxane-free, Sugar-free, PFOS-free, Fungicide-free, Perfluorocarbon (PFC)-free, BSE-free, Natural Latex Rubber-Free, Impurities-free, Vegan, Low Odor
METHOCEL™ 240S HPMC - Specialty is a versatile product used in various pharmaceutical applications, including wet granulation, tablet coating, and granulation. It is suitable for creating tablets, capsules, and suspensions. This product features sewage-sludge-free food ingredients. In the pharma and nutraceutical sectors, it functions as a controlled release agent, immediate release agent, thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive. METHOCEL™ Specialty 240S HPMC is water-soluble, making it highly effective for diverse formulations.
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, 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 - 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.
ETHOCEL™ Standard 100 FP Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 100 FP 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, Dye Free, Kosher, 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, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, 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), FDA 21 CFR 573.420, European Regulation 396/2005/EC, 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, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, 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, Tablet Coating, Granulation
ETHOCEL™ Standard 100 FP Premium Ethylcellulose a white powdered ethylcellulose variant, boasts benefits such as controlled release, excellent flexibility, and thermal stability. Its utility extends to cosmetic applications, where it functions as a stabilizer and thickener. Its manufacturing technology includes direct compression, encapsulation, granulation, and hot melt extrusion processes.
POLYOX™ WSR - 1105 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 1105 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, 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, 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 - 1105 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.
Protanal® LF - 10/60LS banner
IFF Pharma SolutionsProtanal® LF - 10/60LS
  • 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 - 10/60LS available in powdered form, offers versatile applications in pharmaceuticals and nutraceuticals. It serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, providing multifunctional support in various formulations.
METHOCEL™ E4M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ E4M Modified Cellulose Food Grade - Specialty
  • INCI Name:Methylcellulose
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Dosage Form:Tablets
  • Ingredient Origin:Plant Origin
  • Labeling Claims:Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, PAH-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Irradiation-free, Animal Products-free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Dairy-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, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free, Antibiotics-free, Pareve
  • Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FDA 21 CFR 101.9, JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, 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, Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), FDA 21 CFR 172.874, Organic Certified, ISO 14001, FDA 21 CFR 175.105, ISO 50001, EC No.1907/2006, Indian Pharmacopeia, FDA 21 CFR 182.1480, FDA 21 CFR 176.180, cGMP, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, Halal, Quality Control BV Netherlands, FDA 21 CFR 176.170, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 2022/1396, FDA 21 CFR 175.300, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, FDA 21 CFR 174.5, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, Regulation (EU) No. 1830/2003
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, 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 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.
Viscarin® PH - 209NF banner
IFF Pharma SolutionsViscarin® PH - 209NF
  • Chemical Name:Carrageenan
  • CAS Number:9000-07-1
  • Dosage Form:Soft Gels
  • Labeling Claims:Monosodium Glutamate (MSG)-free, PFOS-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Antibiotics-free, Colorants-free, Dioxin-free, Animal Products-free, GMO-free, Natural Latex Rubber-Free, COSMOS Approved, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Organic, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free
  • Certifications & Compliance:EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA 21 CFR 177.1520, European Commission Decision 97/534/EC, European Pharmacopeia (Ph. Eur.), FDA 21 CFR 179.26, Regulation (EU) No. 1829/2003, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, ISO 9001, Regulation (EU) No. 1830/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FDA 7 CFR 205.605, Orthodox Union Kosher, ABNT NBR 14725, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, IFRA Compliant
  • Manufacturing Technology:Encapsulation
Viscarin® PH - 209NF utilizes encapsulation technology and is GMO-free, non-GMO, BSE-free, TSE-free, and palm oil-free. It caters to healthcare and pharma markets, particularly in oral drug delivery and care solutions. It serves as both an emulsifier and stabilizer and aids in formulation and processing in pharmaceutical and nutraceutical applications, including modified and controlled release formulations.

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