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53 Products found on IFF Pharma Solutions in Pharmaceuticals & Nutraceuticals

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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.

IFF Pharma SolutionsETHOCEL™ Medium 70 LD Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
Labeling Claims:Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Zero Calorie, PVC-free, Iodide-free, Aluminum-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Not Listed In California Proposition 65, Irradiation-free, Monosodium Glutamate (MSG)-free, Bisphenol Derivatives-free, Odor-free, Phthalates-free, FSSC 22000, Dioxane-free, PHO (Partially Hydrogenated Oil)-Free, PFAS-Free, Caffeine Free, Hormones-free, Preservative-free, Quaternary Ammonium Salt-Free, APE-free, PFOS-free, PFOA-free, VOC-free, Paraben-free, Tributyltin (TBT) - Free, Halal, Non-GMO, Organic, Sewage Sludge Free, Non-Mutagenic, Non-Irritant, Plasticizer-free, Potassium-free, Antibiotics-free
Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, EFSA (European Food Safety Authority) Certified, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, FDA 21 CFR 117, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, Directive 2011/65/EU (RoHS 2), FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), Directive 2012/19/EU, EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, ISO 9000, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), FSC Certified, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Encapsulation, Direct Compression, Tablet Coating, Granulation

ETHOCEL™ Medium 70 LD Premium Ethylcellulose finds utility in granulation, tablet coating, spray, phenolics, modified rosins, and alkyds (Long Oil). It acts as a thickener, binder, controlled release agent, and granulation aid, ensuring consistent performance across various applications. Its premium quality and versatility make it an essential component in industrial processes.

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.

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 N60K LEO NF Grade - Specialty banner

IFF Pharma SolutionsPOLYOX™ WSR N60K LEO NF Grade - Specialty

INCI Name:PEG-45M
Chemical Name:Polyethylene Oxide
Chemical Family:Ethylene Oxide Copolymers, Cellulose Ethers, Cellulose & Cellulosics
Ingredient Origin:Plant Origin, Synthetic
Labeling Claims:Allergen-free, Vegan, Animal Products-free, No Added Formaldehyde, Dairy-free, Irradiation-free, Vegetarian, Zinc-free, BSE-free, Kosher, Ethylene Oxide-free, Plant-Based, Non-GMO, Nitrosamines-free, Halal, Oxidatively Degradable, Residual Solvent -Free, TSE-free, Not Tested on Animals, Ethylene Glycol-free, Diethylene Glycol-free, Naturally Derived, Heavy Metal-free, Chlorine-free

POLYOX™ WSR N60K LEO NF Grade - Specialty 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 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.

IFF Pharma SolutionsPOLYOX™ WSR - N10 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 - N10 LEO NF Grade an off-white powder, is prized for its water solubility, making it an effective binder and thickener in both cleaning and cosmetic products. Its versatility and solubility make it a valuable ingredient for various formulations.

IFF Pharma SolutionsETHOCEL™ Standard 7 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
Dosage Form:Tablets
Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, 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, 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, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Hot Melt Extrusion, Encapsulation, Direct Compression, Tablet Coating, Granulation

ETHOCEL™ Standard 7 Premium Ethylcellulose White Powder has binding, controlled release, flexibility, and thermal stability benefits. It's soluble in organic solvents and ethanol. Used in direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating. It functions as a controlled release agent, granulation aid, and taste masking agent.

IFF Pharma SolutionsETHOCEL™ Standard 7 FP Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
Labeling Claims:Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Zero Calorie, PVC-free, Iodide-free, Aluminum-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Not Listed In California Proposition 65, Irradiation-free, Monosodium Glutamate (MSG)-free, Bisphenol Derivatives-free, Odor-free, Phthalates-free, FSSC 22000, Dioxane-free, PHO (Partially Hydrogenated Oil)-Free, PFAS-Free, Caffeine Free, Hormones-free, Preservative-free, Quaternary Ammonium Salt-Free, APE-free, PFOS-free, PFOA-free, VOC-free, Paraben-free, Tributyltin (TBT) - Free, Halal, Non-GMO, Organic, Sewage Sludge Free, Non-Mutagenic, Non-Irritant, Plasticizer-free, Potassium-free, Antibiotics-free
Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, EFSA (European Food Safety Authority) Certified, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, FDA 21 CFR 117, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, Directive 2011/65/EU (RoHS 2), FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), Directive 2012/19/EU, EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, ISO 9000, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), FSC Certified, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Tablet Coating, Granulation

ETHOCEL™ Standard 7 FP Premium Ethylcellulose is ideal for granulation, tablet coating, spray, phenolics, and modified rosins applications. It boasts excellent adhesion, good green strength, high gloss, and printability. Serving as a thickener, binder, controlled release agent, and granulation aid, it's available in both powder and granule forms. With properties like ethanol and isopropanol solubility, it ensures compatibility with various solvents, catering to diverse industrial needs.

IFF Pharma SolutionsETHOCEL™ Standard 10 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
Dosage Form:Tablets
Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, 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, 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, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Manufacturing Technology:Hot Melt Extrusion, Encapsulation, Direct Compression, Tablet Coating, Granulation

ETHOCEL™ Standard 10 Premium Ethylcellulose characterized by its white color, serves as a stabilizer and thickener in cosmetic ingredients. Utilizing encapsulation, granulation, hot melt extrusion, and tablet coating technologies, it is available in a powdered physical form.

POLYOX™ WSR 301 LEO NF Grade - Specialty banner

IFF Pharma SolutionsPOLYOX™ WSR 301 LEO NF Grade - Specialty

INCI Name:PEG-90M
Chemical Name:Polyethylene Oxide
Chemical Family:Ethylene Oxide Copolymers, Cellulose Ethers, Cellulose & Cellulosics
Ingredient Origin:Non-Animal Origin, Plant Origin, Synthetic
Labeling Claims:Allergen-free, Vegan, Animal Products-free, No Added Formaldehyde, Dairy-free, Irradiation-free, Vegetarian, Zinc-free, BSE-free, Kosher, Ethylene Oxide-free, Plant-Based, Non-GMO, Nitrosamines-free, Halal, Oxidatively Degradable, Residual Solvent -Free, TSE-free, Not Tested on Animals, Ethylene Glycol-free, Diethylene Glycol-free, Naturally Derived, Heavy Metal-free, Chlorine-free

POLYOX™ WSR 301 LEO NF Grade - Specialty 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.

IFF Pharma SolutionsPOLYOX™ WSR - N60K NF

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), 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 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.

POLYOX™ WSR N750 LEO NF Grade - Specialty banner

IFF Pharma SolutionsPOLYOX™ WSR N750 LEO NF Grade - Specialty

INCI Name:PEG-7M
Chemical Name:Polyethylene Oxide
Chemical Family:Ethylene Oxide Copolymers, Cellulose Ethers, Cellulose & Cellulosics
Ingredient Origin:Plant Origin, Synthetic
Labeling Claims:Allergen-free, Vegan, Animal Products-free, No Added Formaldehyde, Dairy-free, Irradiation-free, Vegetarian, Zinc-free, BSE-free, Kosher, Ethylene Oxide-free, Plant-Based, Non-GMO, Nitrosamines-free, Halal, Oxidatively Degradable, Residual Solvent -Free, TSE-free, Not Tested on Animals, Ethylene Glycol-free, Diethylene Glycol-free, Naturally Derived, Heavy Metal-free, Chlorine-free

POLYOX™ WSR N750 LEO NF Grade - Specialty 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.

IFF Pharma SolutionsPOLYOX™ WSR - 1105 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 - 1105 LEO NF Grade an off-white powder, serves as a binder and thickener in cleaning agents. It is available in powder form and is water-soluble, making it suitable for use in gels and osmotic pump tablets.

ETHOCEL™ Medium 70 LD Industrial Ethylcellulose - Specialty banner

IFF Pharma SolutionsETHOCEL™ Medium 70 LD Industrial Ethylcellulose - Specialty

Chemical Name:Ethylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
CAS Number:9004-57-3
Dosage Form:Tablets
Labeling Claims:Endocrine Disruptor-free, VOC-free, PAH-free, Plasticizer-free, Tributyl Tin Compounds-Free, Formaldehyde-free, Kosher, Phthalates-free, Monosodium Glutamate (MSG)-free, Dairy-free, Caffeine Free, Palm Oil-free, Halal, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, Zero Calorie, Irradiation-free, Aflatoxin-free, Hormones-free, Glycerin-free, Dye Free, 1,4-Dioxane-free, Colorants-free, Preservative-free, Sewage Sludge Free, Natural Latex Rubber-Free, TSE-free, Pesticide-free, BSE-free, Organic, Sugar-free, APE-free, PFAS-Free, Allergen-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Antibiotics-free, Bisphenol A-free, Mycotoxins-free, Aluminum-free, Dioxin-free, PVC-free, PFOS-free, Paraben-free
Certifications & Compliance:European Regulation 396/2005/EC, ISO 9001, RoHS 2 Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 1169/2011, GMP, FDA Food Safety Modernization Act (FSMA), FCC Compliant, Majelis Ulama Indonesia Halal, Regulation (EU) No. 10/2011 (PIM), Japan Chemical Substances Control Law (CSCL), Japan Pharmacopeia (JP), Turkish RoHS Regulation, Canadian Environmental Protection Act (CEPA), Swiss Ordinance (SR 817.023.21), EuPIA Listed, USDA Organic, Doping-Free, Directive 2009/48/EC, FDA 21 CFR 163, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, FDA 21 CFR 181.24, FSSC 22000, cGMP, European Pharmacopeia (Ph. Eur.), ICH Q3C, WEEE Directive 2012/19/EU, Organic Certified, Directive 2023/915/EU, EC No.1907/2006, Regulation (EU) No. 231/2012, RoHS Compliant, FDA 21 CFR 101.9, Clean Air Act (CAA) Certified, Regulation (EU) No. 1272/2008, Indian Pharmacopeia, Kosher, EU Cosmetic Regulation 1223/2009 Compliant
Manufacturing Technology:Granulation, Encapsulation, Tablet Coating, Direct Compression

ETHOCEL™ Medium 70 LD Industrial Ethylcellulose - Specialty boasts binding, controlled release, flexibility, and thermal stability. It's compatible with hot melt coating and serves as a stabilizer and thickener in cosmetics. The labeling touts it as palm oil-free, glycerin-free, and endocrine disruptor-free. It dissolves in ethanol and organic solvents.

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