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IFF Pharma Solutions

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164 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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Protanal® CR - 8133 banner
IFF Pharma SolutionsProtanal® CR - 8133
  • 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, Odor-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® CR - 8133 featuring sodium alginate, serves various functions in pharmaceuticals and nutraceuticals. It acts as controlled release agent, emulsifying agent, gelling agent, thickener, and viscosity modifier, available in powder form.
ETHOCEL™ Standard 14 Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 14 Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Controlled Release Agent, Granulation Aid, Binder, Taste Masker
  • 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, 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), 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, EC No. 1935/2004, 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, 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, EC No. 2023/2006, 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), EU Directive 2002/72/EC, GMP
  • Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Encapsulation, Direct Compression
ETHOCEL™ Standard 14 Premium Ethylcellulose available in powder form, is adaptable for various manufacturing processes such as direct compression, encapsulation, and granulation. It exhibits ethanol solubility, offering versatility in pharmaceutical and industrial applications.
Manugel® DMB banner
IFF Pharma SolutionsManugel® DMB
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free, Halal, Paraben-free, Formaldehyde-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Copper-free, PFOS-free, Residual Solvent -Free, Heavy Metal-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Antibiotics-free, Melamine-free, Barium-free, Cadmium-free, Colorants-free, Latex-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, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free
  • Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS)
Manugel® DMB is free from copper, cobalt, barium, and gold. It serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications.
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.
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.
ETHOCEL™ Standard 7 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 7 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:Caffeine Free, Organic, Irradiation-free, VOC-free, Quaternary Ammonium Salt-Free, PFOS-free, Dioxane-free, Dairy-free, Odor-free, Tributyltin (TBT) - Free, Allergen-free, Natural Latex Rubber-Free, Zero Calorie, Nitrosamines-free, Bisphenol Derivatives-free, Pesticide-free, Non-GMO, Kosher, Hormones-free, APE-free, Sugar-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, FSSC 22000, PHO (Partially Hydrogenated Oil)-Free, Iodide-free, Gluten-free, Sewage Sludge Free, Paraben-free, Phthalates-free, Dye Free, 1,4-Dioxane-free, PAH-free, Halal, Preservative-free, PVC-free, Potassium-free, PFOA-free, Aluminum-free, PFAS-Free, Antibiotics-free, Non-Irritant, Non-Mutagenic
  • Color (Properties):White
  • Certifications & Compliance:FDA 21 CFR 101.9, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, ISO 9001, Organic Certified, cGMP, GMP, Directive 1333/2008/EC, ICH Q3C, Directive 2011/65/EU (RoHS 2), FSSC 22000, United States Pharmacopeia (USP), EFSA (European Food Safety Authority) Certified, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 172.868, FSC Certified, FDA Food Safety Modernization Act (FSMA), JECFA (FAO/WHO), RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), EuPIA Listed, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Regulation (EU) No. 1272/2008, Directive 2012/19/EU, Directive 2009/48/EC, Halal, USDA Organic, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), Kosher, FDA 21 CFR 117, Chinese Pharmacopeia (ChP), EC No.1907/2006
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 7 Industrial Ethylcellulose - Specialty is designed for spray, phenolics, and modified rosins applications. Noted for its high gloss and good printability, it functions as a thickener, rheology modifier, and binder & resin. Available in powder or granule form, it's white in color, offering versatility in industrial processes.
ETHOCEL™ Standard 10 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 10 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:Caffeine Free, Organic, Irradiation-free, VOC-free, Quaternary Ammonium Salt-Free, PFOS-free, Dioxane-free, Dairy-free, Odor-free, Tributyltin (TBT) - Free, Allergen-free, Natural Latex Rubber-Free, Zero Calorie, Not Listed In California Proposition 65, Nitrosamines-free, Bisphenol Derivatives-free, Pesticide-free, Non-GMO, Kosher, Hormones-free, APE-free, Sugar-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, FSSC 22000, PHO (Partially Hydrogenated Oil)-Free, Iodide-free, Gluten-free, Sewage Sludge Free, Paraben-free, Phthalates-free, Dye Free, 1,4-Dioxane-free, PAH-free, Halal, Preservative-free, PVC-free, Potassium-free, PFOA-free, Aluminum-free, PFAS-Free, Antibiotics-free, Non-Irritant, Non-Mutagenic
  • Color (Properties):White
  • Certifications & Compliance:FDA 21 CFR 101.9, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, ISO 9001, Organic Certified, cGMP, GMP, Directive 1333/2008/EC, ICH Q3C, Directive 2011/65/EU (RoHS 2), FSSC 22000, United States Pharmacopeia (USP), EFSA (European Food Safety Authority) Certified, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 172.868, FSC Certified, FDA Food Safety Modernization Act (FSMA), JECFA (FAO/WHO), RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), EuPIA Listed, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Regulation (EU) No. 1272/2008, Directive 2012/19/EU, Directive 2009/48/EC, Halal, USDA Organic, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), Kosher, FDA 21 CFR 117, Clean Water Act (CWA) Certified, Chinese Pharmacopeia (ChP), EC No.1907/2006
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 10 Industrial Ethylcellulose - Specialty is tailored for modified rosins, alkyds (Long Oil), and phenolics. With benefits like being aluminum-free, antibiotics-free, APE-free, bisphenol derivatives-free, caffeine-free, and dioxane-free, it ensures product purity and safety. Notable features include scuff resistance, serving as a stabilizer, thickener, rheology modifier, binder & resin, and film former, guaranteeing optimal performance in various industrial applications.
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.

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