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IFF Pharma Solutions

Excipients
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32 Products found on IFF Pharma Solutions  in Excipients

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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, 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 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.
Avicel® PH - 102SCG banner
IFF Pharma SolutionsAvicel® PH - 102SCG
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Granules, Suspension
  • Labeling Claims:Genotoxic-free, Plasticizer-free, Halal, PFOA-free, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Tributyltin (TBT) - Free, Monosodium Glutamate (MSG)-free, Diethylene Glycol-free, Iodide-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Impurities-free, Antibiotics-free, Melamine-free, Fragrance allergen-free, Amine-free, Latex-free, Potassium-free, Fungicide-free, Dioxin-free, Dioxane-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, Bisphenol Derivatives-free, PFAS-Free, Herbicide-free, Non-GMO, PAH-free, Not Tested on Animals, TSE-free, Palm Oil-free, Vegetarian, Pareve, Quaternary Ammonium Salt-Free, Ethylene Oxide-free, Ethylene Glycol-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, CMR Substances-free, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Endocrine Disruptor-free, Glycerin-free
  • Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), Kosher, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Clean Water Act (CWA) Certified, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Nagoya Compliant, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, FDA 21 CFR 117, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher, Orthodox Union Kosher
  • Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression
Avicel® PH - 102SCG is a microcrystalline cellulose used in direct compression, dry granulation, and wet granulation manufacturing technologies. It is essential for producing high-quality pharmaceutical tablets with optimal stability and performance.
POLYOX™ WSR - N12K LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K LEO NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, 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 - N12K LEO NF Grade is an off-white powder with water-soluble properties. It's used as a binder and thickener in cleaning products and pharmaceuticals. Its applications include gels, osmotic pump tablets, and regular tablets, and it's manufactured using direct compression technology. Additionally, it serves as a controlled release agent.
Avicel® SMCC - 50 banner
IFF Pharma SolutionsAvicel® SMCC - 50
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Tablets
  • Labeling Claims:Triphenyl Tin Compounds-Free, Genotoxic-free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Zinc-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Impurities-free, Antibiotics-free, Melamine-free, Colorants-free, Amine-free, Latex-free, Dioxin-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Not Tested on Animals, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Perfluorooctanoic Acid-free, Glycerin-free
  • Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1272/2008, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), Kosher, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher, Orthodox Union Kosher
  • Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression
Avicel® SMCC - 50 is used in tablet formulations, employing various manufacturing technologies like direct compression, dry granulation, and wet granulation. It serves multiple functions in pharmaceutical and nutraceutical applications, including acting as a binder, compression aid, filler, and immediate release agent.
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, 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 - 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 - 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, 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 - 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 - N10 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N10 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, 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 - N10 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.
Viscarin® PH - 109NF banner
IFF Pharma SolutionsViscarin® PH - 109NF
  • 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, 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 - 109NF employing encapsulation technology, offers BSE-free, TSE-free, palm oil-free, and glycerin-free formulations. It serves as a controlled release agent, encapsulant, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications.
Avicel® PH - 101 banner
IFF Pharma SolutionsAvicel® PH - 101
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Pellets, Orally Disintegrating Tablets (ODTs), Tablets, Capsules, Granules, Effervescent Tablets
  • Labeling Claims:Generally Recognized As Safe (GRAS), Vegan, Kosher, BSE-free, GMO-free, Halal, TSE-free, Vegetarian, Pareve
  • Certifications & Compliance:EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), Kosher, Halal, Halal, Central Islamic Council of Thailand, National Formulary (NF), FSSC 22000, cGMP, IFANCA Halal, EXCiPACT, ISO 9001, Halal Food Council of Europe
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
Microcrystalline Cellulose is purified, partially depolymerized cellulose prepared by treating alpha cellulose obtained as a pulp from fibrous plant material with mineral acids. Several grades of Avicel® PH MCC are available varying in particle size distribution, density and moisture content. Avicel® PH microcrystalline cellulose (MCC) is most often used as a compression Aid, filler, flow aid, and dry binder for tablets and capsules. Avicel® PH-101 has a typical average particle size of 50 µm and moisture content between 3 and 5%. Avicel® PH-101 is primarily used for wet granulation, extrusion spherization and tablet compression. Avicel® PH MCC rapidly absorbs aqueous binder solution permitting faster addition of fluid as well as shorter wet massing time. At the same time, the water does not become bound water resulting in faster drying time and uniform granular properties.
Gelcarin® PH - 911 banner
IFF Pharma SolutionsGelcarin® PH - 911
  • Chemical Name:Carrageenan
  • CAS Number:9000-07-1
  • Labeling Claims:Preservative-free, 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, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, TSE-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, Triphenyl Tin Compounds-Free, Plasticizer-free, Halal, Paraben-free, Aluminum-free
  • Certifications & Compliance:IFRA Compliant, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Kosher, Halal, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FCC Compliant, British Pharmacopeia (BP), Orthodox Union Kosher, FSSC 22000, cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008
  • Manufacturing Technology:Encapsulation
Gelcarin® PH - 911 Non-animal origin carrageenan is utilized in encapsulation. It functions as a controlled release agent, emulsifying agent, gelling agent, stabilizer, and thickener in pharmaceuticals and nutraceuticals.
Avicel® SMCC HD 90 banner
IFF Pharma SolutionsAvicel® SMCC HD 90
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Labeling Claims:Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Zinc-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Solvent-free, Impurities-free, Antibiotics-free, Melamine-free, Colorants-free, Amine-free, Latex-free, Dioxin-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, PFAS-Free, Non-GMO, PAH-free, Not Tested on Animals, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Genotoxic-free, Plasticizer-free
  • Certifications & Compliance:Regulation (EU) No. 1272/2008, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), Kosher, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher, Orthodox Union Kosher, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
Avicel® SMCC HD 90 comprising non-animal origin microcrystalline cellulose, is utilized in various pharmaceutical and nutraceutical applications. Employing direct compression, dry granulation, and wet granulation manufacturing technologies, it serves as a compression aid, filler, and immediate release agent.
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, 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 - 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 - 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, 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 - 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.

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