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IFF Pharma Solutions
PRONOVA® SLG100
Chemical Name:
Sodium Alginate
Dosage Form:
Foams
Labeling Claims:
Kosher, Not Listed In California Proposition 65, Biocompatible, High Purity, Halal
Certifications & Compliance:
Clean Water Act (CWA) Certified, ISO 14001, National Formulary (NF), SARA 311/312, Hazard Analysis Critical Control Point (HACCP), European Pharmacopeia (Ph. Eur.), ISO 9000, SARA 313, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), United States Pharmacopeia (USP), GMP, Directive 2023/2055/EU, EC No.1907/2006
Manufacturing Technology:
Encapsulation
PRONOVA® SLG100 is available in the form of foams. It serves as an encapsulant and gelling agent. The product is offered in powder and solid forms, catering to various pharmaceutical and nutraceutical applications, including emulsifiers and stabilizers and modified and controlled-release excipients.
IFF Pharma Solutions
Lattice® NT-020 - Specialty
Chemical Family:
Cellulose & Cellulosics
Labeling Claims:
Artificial Flavor-Free, Odor-free, Latex-free, Allergen-free, Irradiation-free, VOC-free, Dioxin-free, Not Listed In California Proposition 65, Halal, TSE-free, BSE-free, Pesticide-free, Aflatoxin-free, Kosher, Non-Toxic
Certifications & Compliance:
FDA 40 CFR 122.21, ISO 22000, FDA 40 CFR 122.42, Generally Recognized As Safe (GRAS), FCC Compliant, FDA 21 CFR 117, ISO 45001, Clean Water Act (CWA) Certified, ISO 14001, Halal Food Council of Europe, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), ICH Q3C, ISO 9001
Lattice® NT-020 - Specialty is formulated for tablet production and suitable for direct compression and wet granulation methods. With minimal residue, it acts as a binder, ensuring tablet cohesion. Identified as cellulose and cellulosics, specifically microcrystalline cellulose, it offers water-dispersible granules (WDG) and is available in powder form for versatile formulation options.
IFF Pharma Solutions
POLYOX™ WSR - N12K NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Thickener, Flocculant, Film Former, Viscosity Modifier, Lubricant, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
POLYOX™ WSR - 303 NF TG LEO
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
Manufacturing Technology:
Direct Compression
POLYOX™ WSR - 303 NF TG LEO featuring an off-white color and a powder physical form, serves as a binder and thickener in various cleaning applications. It is formulated for use in gels, osmotic pump tablets, and conventional tablets, offering water solubility for effective performance.
IFF Pharma Solutions
Scogin® MV - Specialty
Chemical Family:
Alginates
Labeling Claims:
Not Listed In California Proposition 65, Halal, Organic, Biodegradable, Odor-free, Biorenewable
Physical Form:
Powder
Scogin® MV - Specialty recognised as both alginates and sodium alginate, excels as a film former while also serving as a gelling agent and thickener. Available in brown or yellow powder forms, it offers cold water solubility, ensuring ease of use in various applications. Its versatility and effectiveness make it a preferred choice for formulations requiring film-forming properties.
IFF Pharma Solutions
Protacid® F120
Chemical Name:
Alginic Acid
CAS Number:
9005-32-7
Labeling Claims:
Steroids Free, Butylated Hydroxyanisole-free, Not Listed In California Proposition 65, Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Halal, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, NPE-free, Benzoates-free, Pareve, Herbicide-free, Solvent-free, Perfluorocarbon (PFC)-free, Residual Solvent -Free, APE-free, Caffeine Free, Glutamate-Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Azo Dyes-free, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Bactericide-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Radioactive-free, GMO-free, Kosher, Preservative-free, PFAS-Free, Conflict minerals-free, Nanomaterials-free, Potassium-free, Vegan
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), GMP, FDA 21 CFR 117, Halal, Clean Water Act (CWA) Certified, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), FDA 21 CFR 582.7724, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FFDCA, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1169/2011
Protacid® F120 is a sewage sludge-free, controlled-release agent ideal for pharmaceutical and nutraceutical applications. Additionally, it functions as an antacid, ensuring optimal performance in various formulations.
IFF Pharma Solutions
POLYOX™ WSR - N60K NF
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
Manufacturing Technology:
Direct Compression
POLYOX™ WSR - N60K NF 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.
IFF Pharma Solutions
POLYOX™ WSR - N80 FP NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Thickener, Flocculant, Film Former, Viscosity Modifier, Lubricant, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
Manufacturing Technology:
Direct Compression
POLYOX™ WSR - N80 FP 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.
IFF Pharma Solutions
METHOCEL™ F50 PVC HPMC - Specialty
Functions:
Controlled Release Agent, Rheology Modifier
Chemical Name:
Hydroxypropyl Methylcellulose
Chemical Family:
Cellulose & Cellulosics, Cellulose Ethers
Labeling Claims:
Natural Latex Rubber-Free, Phthalates-free, Hormones-free, VOC-free, Generally Recognized As Safe (GRAS), TSE-free, Aflatoxin-free, Irradiation-free, PVC-free, Nitrosamines-free, 1,4-Dioxane-free, APE-free, Caffeine Free, Paraben-free, Vegan, PAH-free, Halal, Kosher, Mycotoxins-free, Sewage Sludge Free, CMR Substances-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Triphenyl Tin Compounds-Free, Naturally Derived, Sugar-free, Not Listed In California Proposition 65, Glycerin-free, Plant-Based, Dairy-free, Organic, Monosodium Glutamate (MSG)-free, Pesticide-free, Aluminum-free, Non-GMO, PFAS-Free, Vegetarian, Antibiotics-free, BSE-free, Bisphenol A-free, PFOS-free, Dye Free, Palm Oil-free, Preservative-free, Perfluorooctanoic Acid-free, Colorants-free, Plasticizer-free, Tributyl Tin Compounds-Free
Certifications & Compliance:
European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), ISO 9001, RoHS 2 Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, FDA 21 CFR 182.1480, Regulation (EU) No. 1829/2003, EU Packaging Directive (94/62/EC), ISO 50001, USDA Organic, Turkish RoHS Regulation, Regulation (EC) No. 1333/2008, Halal, Directive 1333/2008/EC, Doping-Free, Directive 2009/48/EC, Majelis Ulama Indonesia Halal, Chinese Pharmacopeia (ChP), FDA Compliant, cGMP, ISO 14001, FSSC 22000, FDA 21 CFR 172.874, JECFA (FAO/WHO), European Pharmacopeia (Ph. Eur.), Clean Water Act (CWA) Certified, Swiss Ordinance (SR 817.023.21), WEEE Directive 2012/19/EU, Regulation (EU) No. 2022/1396, Organic Certified, Directive 2023/915/EU, Regulation (EU) No. 1830/2003, Regulation (EU) No. 231/2012, RoHS Compliant, FEMA Compliant, Kosher, FDA 21 CFR 101.9, Orthodox Union Kosher, Clean Air Act (CAA) Certified, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant
Dosage Form:
Tablets
METHOCEL™ F50 PVC HPMC - Specialty a cellulose ether derivative known as hypromellose, acts as a rheology modifier in industrial applications. Sourced from plants, it boasts water solubility, making it versatile for various formulations.
IFF Pharma Solutions
POLYOX™ WSR - N80 NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
POLYOX™ WSR - 303 FP NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
Manufacturing Technology:
Direct Compression
POLYOX™ WSR - 303 FP 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.
IFF Pharma Solutions
POLYOX™ WSR N 80NF TG LEO
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Thickener, Flocculant, Film Former, Viscosity Modifier, Lubricant, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
Manufacturing Technology:
Direct Compression
POLYOX™ WSR N 80NF TG LEO, in an off-white powder form, serves as a binder and thickener in cleaning and pharmaceutical formulations. Its water solubility makes it suitable for various applications, while its direct compression manufacturing technology ensures efficient production processes. Additionally, it functions as a controlled release agent, adding value to pharmaceutical formulations.
IFF Pharma Solutions
Protaweld® S 200 - Specialty
Chemical Family:
Alginates
End Uses:
Welding Electrodes
Protaweld® S 200 - Specialty essential for welding electrodes, boasts sodium alginate and sucrose. Recognised for stability, it ensures efficient welding operations. Available in powder form, it facilitates easy integration into various welding applications, providing robust performance and reliability to welding professionals.
IFF Pharma Solutions
POLYOX™ WSR - 303 NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Thickener, Flocculant, Film Former, Viscosity Modifier, Lubricant, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
Scogin® LV - Specialty
Chemical Family:
Alginates
Labeling Claims:
Not Listed In California Proposition 65, Organic, Biodegradable, Kosher, Odor-free, Biorenewable
Physical Form:
Powder
Scogin® LV - Specialty identified as alginates and sodium alginate, is renowned for its excellent film-forming qualities. Acting as both a gelling agent and thickener, it ensures optimal performance across applications. Available in brown or yellow powder forms, it exhibits cold and hot water solubility, providing versatility in formulation processes.
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