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IFF Pharma Solutions

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167 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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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, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 303 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.
Avicel® CE-15 banner
IFF Pharma SolutionsAvicel® CE-15
  • Chemical Name:Guar Gum, Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
  • Dosage Form:Tablets, Soft Chews
  • Labeling Claims:Perfluorooctanoic Acid-free, Triphenyl Tin Compounds-Free, Genotoxic-free, Not Engineered With Nanomaterials, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, Aflatoxin-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Melamine-free, Colorants-free, Amine-free, Latex-free, Dioxin-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Artificial Flavor-Free, Non-GMO, PAH-free, Not Tested on Animals, Perchlorate-free, Tributyl Tin Compounds-Free, TSE-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
  • Certifications & Compliance:Directive 1895/2005/EC, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1169/2011, IFRA Compliant, Halal Food Council of Europe, EC No. 1935/2004, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), EC No. 2023/2006, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, EU Directive 2002/72/EC, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, Regulation (EU) No. 10/2011 (PIM), EU Cosmetic Regulation 1223/2009 Compliant, Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, FCC Compliant, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher, Orthodox Union Kosher
  • Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression
Avicel® CE-15 a non-animal-derived ingredient, is widely employed in tablet production. It's adaptable to various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceutical and nutraceutical applications, it acts as a binder, compression aid, filler, immediate release agent, and suspension aid. It's supplied in powder form for easy tablet formulation.
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, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 303 NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.
Protanal® KF200 RBS banner
IFF Pharma SolutionsProtanal® KF200 RBS
  • Chemical Name:Potassium Alginate
  • CAS Number:9005-36-1
  • 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)
Protanal® KF200 RBS available in powder form, serves multiple functions in pharmaceuticals and nutraceuticals. It acts as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, offering versatile applications in various formulations.
Viscarin® SD - 339 banner
IFF Pharma SolutionsViscarin® SD - 339
  • 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, 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, 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
  • 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, Clean Water Act (CWA) Certified, 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, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA)
  • Manufacturing Technology:Encapsulation
Viscarin® SD - 339 made with encapsulation tech, is aluminum, antibiotics, APE, and bisphenol A-free. It's key in healthcare, particularly pharmaceutical manufacturing. In food, it acts as an emulsifier, stabilizer, thickener, and texturizer, enhancing consistency. Available as powder, it's versatile.
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, 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 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.
Gelcarin® GP - 812 banner
IFF Pharma SolutionsGelcarin® GP - 812
  • 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, Not Listed In California Proposition 65, 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® GP - 812 composed of carrageenan, is manufactured using encapsulation technology. It serves multiple functions in pharmaceuticals and nutraceuticals, including as a controlled-release agent, emulsifying agent, gelling agent, stabilizer, and thickener.
Protacid® AR - 1112 banner
IFF Pharma SolutionsProtacid® AR - 1112
  • Chemical Name:Alginic Acid
  • CAS Number:9005-32-7
  • Functions:Antacid, Controlled Release Agent
  • Labeling Claims:Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Dye Free, Kosher, Propylene Glycol-free, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), Solvent-free, PAH-free, Allergen-free, Residual Solvent -Free, Irradiation-free, Animal Products-free, Melamine-free, Latex-free, Monosodium Glutamate (MSG)-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, Tributyl Tin Compounds-Free, APE-free, PFOS-free, BSE-free, Paraben-free, Halal, Non-GMO, GMO-free, Nanomaterials-free, Plasticizer-free, Antibiotics-free, Pareve
  • Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), ISO 14001, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Kosher, National Formulary (NF), Halal Food Council of Europe, EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, ISO 9000, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, Regulation (EU) No. 1830/2003
  • Chemical Inventories:PICCS (Phillipines)
Protacid® AR - 1112 primarily composed of alginic acid, offers various benefits, such as being free of APE, bisphenol A, caffeine, and colorants. In pharmaceutical and nutraceutical applications, it functions as an antacid and controlled release agent. Its physical form is a powder, ensuring ease of handling and formulation.
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, 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 - 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.
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, 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 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.

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