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Pharmaceutical Actives & Precursors

Excipients

Pharmaceutical Actives & Precursors

152 Products found on IFF Pharma Solutions in Pharmaceuticals & Nutraceuticals

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METHOCEL™ F4M Premium HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F4M Premium HPMC - Specialty

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, Hypoallergenic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, Generally Recognized As Safe (GRAS), PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, VOC-free, TSE-free, Pareve, Perfluorooctanoic Acid-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, Mycotoxins-free, Kosher, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, APE-free, Pesticide-free, Triphenyl Tin Compounds-Free, CMR Substances-free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan, Low Odor

METHOCEL™ F4M Premium HPMC - Specialty is water-soluble and finds application in ceramics and pharmaceuticals. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, suspension aid, thickener, and viscosity modifier. Produced through granulation, it serves various industrial and pharmaceutical functions.

METHOCEL™ K4M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K4M Modified Cellulose Food Grade - Specialty

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Dairy-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, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free, Antibiotics-free, Pareve
Certifications & Compliance:Japan Pharmacopeia (JP), FDA 21 CFR 101.9, Swiss Ordinance (SR 817.023.21), JECFA (FAO/WHO), FEMA Compliant, European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), FDA 21 CFR 172.874, Organic Certified, ISO 14001, FDA 21 CFR 175.105, ISO 50001, EC No.1907/2006, Indian Pharmacopeia, FDA 21 CFR 182.1480, FDA 21 CFR 176.180, cGMP, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, Halal, Quality Control BV Netherlands, FDA 21 CFR 176.170, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 2022/1396, FDA 21 CFR 175.300, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, FDA 21 CFR 174.5, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, Regulation (EU) No. 1830/2003

METHOCEL™ K4M Modified Cellulose Food Grade - Specialty a food-grade product, acts as a binder, controlled release agent, film former, and gelling agent in pharmaceuticals and nutraceuticals. It facilitates granulation and tablet coating processes and exhibits water solubility.

IFF Pharma SolutionsMETHOCEL™ F50 HPMC - Specialty

INCI Name:Methylcellulose, Hydroxypropyl Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Non-GMO, Palm Oil-free, Phthalates-free, Paraben-free, Nitrosamines-free, Aluminum-free, Mycotoxins-free, Kosher, Preservative-free, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Halal, Hormones-free, PVC-free, Naturally Derived, Organic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, APE-free, Pesticide-free, Triphenyl Tin Compounds-Free, Generally Recognized As Safe (GRAS), CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Plasticizer-free, Dairy-free, VOC-free, Irradiation-free, TSE-free, Glycerin-free, 1,4-Dioxane-free, Pareve, Sugar-free, PFOS-free, Perfluorooctanoic Acid-free, BSE-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Natural Latex Rubber-Free, Dioxin-free, Vegetarian, Tributyl Tin Compounds-Free, Vegan

METHOCEL™ F50 HPMC - Specialty is a versatile industrial additive that serves as a rheology modifier. It belongs to the cellulose ether chemical family and is derived from plant-based hypromellose. Its water solubility makes it suitable for various applications across different industries.

IFF Pharma SolutionsProtacid® F120 NM

Chemical Name:Alginic Acid, Algin
CAS Number:9005-38-3
Labeling Claims:Monosodium Glutamate (MSG)-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Colorants-free, Dioxin-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Palm Oil-free, Pareve, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-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, Preservative-free
Certifications & Compliance:EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, Directive 2001/18/EC, GMP, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008

Protacid® F120 NM is free from dyes, hormones, monosodium glutamate (MSG), natural latex rubber, polycyclic aromatic hydrocarbons (PAHs), and parabens. Its chemical name is algin.

IFF Pharma SolutionsAquacoat® ECD - 30

Chemical Name:Ethylcellulose
Dosage Form:Tablets
Labeling Claims:Hormones-free, Phthalates-free, Colorants-free, Paraben-free, Natural Latex Rubber-Free, Vegan, Halal, Triphenyl Tin Compounds-Free, Kosher, Ethylene Oxide-free, Non-GMO, PHO (Partially Hydrogenated Oil)-Free, Latex-free, Plasticizer-free, PAH-free, Pesticide-free, GMO-free, Palm Oil-free, Sugar-free, APE-free, Dye Free, PFAS-Free, Generally Recognized As Safe (GRAS), Vegetarian, Aluminum-free, Endocrine Disruptor-free, PVC-free, TSE-free, Not Listed In California Proposition 65, PFOS-free, Allergen-free, Pareve, Genotoxic-free, Perfluorooctanoic Acid-free, Preservative-free, Tributyl Tin Compounds-Free, Nitrosamines-free, Melamine-free, BSE-free, Not Tested on Animals, Glycerin-free, Bisphenol A-free, Dioxin-free, Caffeine Free, Antibiotics-free, Amine-free, Heavy Metal-free, Monosodium Glutamate (MSG)-free, Nanomaterials-free
Certifications & Compliance:cGMP, Nagoya Compliant, EXCiPACT, Regulation (EU) No. 231/2012, Chinese Pharmacopeia (ChP), European Regulation 396/2005/EC, FSSC 22000, ISO 9001, FDA Food Safety Modernization Act (FSMA), European Pharmacopeia (Ph. Eur.), GMP, FCC Compliant, Doping-Free, Japan Pharmacopeia (JP), United States Pharmacopeia (USP), IFANCA Halal, British Pharmacopeia (BP), Orthodox Union Kosher, EC No.1907/2006, National Formulary (NF), FDA Compliant, FDA 21 CFR Regulations

Aquacoat® ECD - 30 containing ethylcellulose, is a liquid formulation utilized for tablet coating. With labeling claims of being palm oil-free, glycerin-free, and endocrine disruptor-free, it serves as a controlled release agent, enteric coating system, sustained release agent, and taste masking agent in pharmaceutical and nutraceutical applications.

METHOCEL™ J12M S HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ J12M S HPMC - Specialty

INCI Name:Methylcellulose, Hydroxypropyl Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
Labeling Claims:Phthalates-free, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Allergen-free, Halal, Potassium-free, PAH-free, Caffeine Free, Sewage Sludge Free, Herbicide-free, PFOA-free, Diethylene Glycol-free, Gluten-free, PHO (Partially Hydrogenated Oil)-Free, Persistent Organic Pollutants (POP)-free, Monosodium Glutamate (MSG)-free, Dairy-free, VOC-free, TSE-free, Pareve, Aflatoxin-free, Endocrine Disruptor-free, Quaternary Ammonium Salt-Free, Iodide-free, Latex-free, Vegetarian, Non-GMO, Palm Oil-free, Ethylene Glycol-free, Mycotoxins-free, Kosher, Dye Free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Organic, Tributyltin (TBT) - Free, APE-free, Pesticide-free, Bisphenol Derivatives-free, CMR Substances-free, Dioxane-free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, Not Listed In California Proposition 65, PFOS-free, Fungicide-free, BSE-free, Natural Latex Rubber-Free, Vegan

METHOCEL™ J12M S HPMC - Specialty identified as cellulose ethers and hypromellose, acts as a rheology modifier, ensuring consistency in formulations. It possesses the property of being water-soluble, making it suitable for various applications.

METHOCEL™ E4M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ E4M Modified Cellulose Food Grade - Specialty

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, PAH-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Irradiation-free, Animal Products-free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Dairy-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, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free, Antibiotics-free, Pareve
Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FDA 21 CFR 101.9, JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), FDA 21 CFR 172.874, Organic Certified, ISO 14001, FDA 21 CFR 175.105, ISO 50001, EC No.1907/2006, Indian Pharmacopeia, FDA 21 CFR 182.1480, FDA 21 CFR 176.180, cGMP, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Regulation (EU) No. 1169/2011, FFDCA, Halal, Quality Control BV Netherlands, FDA 21 CFR 176.170, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 2022/1396, FDA 21 CFR 175.300, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, FDA 21 CFR 174.5, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, Regulation (EU) No. 1830/2003

METHOCEL™ E4M Modified Cellulose Food Grade - Specialty is water-soluble and used in granulation and tablet coating manufacturing. It functions as a binder, controlled release agent, film former, gelling agent, immediate release agent, mucoadhesive, and solubilizer in pharmaceuticals and nutraceuticals.

IFF Pharma SolutionsAvicel® PH - 105

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Functions:Binder
Labeling Claims:Kosher, Pareve, Halal
Certifications & Compliance:Halal Food Council of Europe, FSSC 22000, IFANCA Halal, EC No.1907/2006, Chinese Pharmacopeia (ChP), ISO 9001

Avicel® PH 105 is a fine microcrystalline cellulose excipient optimized for binding applications in tablet formulations, widely utilized in pharmaceuticals and nutraceuticals. This high-performance binder supports robust tablet formation, ensuring effective disintegration and consistent release profiles. Its microcrystalline structure enhances blending and compressibility, making it a reliable choice for uniformity and quality in tablet manufacturing.

IFF Pharma SolutionsAc-Di-Sol® SD - 711

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Orally Disintegrating Tablets (ODTs), Capsules, Granules
Labeling Claims:Generally Recognized As Safe (GRAS), Vegan, Kosher, BSE-free, Non-GMO, Halal, TSE-free, Vegetarian, Pareve
Certifications & Compliance:EC No.1907/2006, Halal, Japan Pharmacopeia (JP), National Formulary (NF), FSSC 22000, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), IFANCA Halal, EXCiPACT, ISO 9001, Kosher
Manufacturing Technology:Wet Granulation

Ac-Di-Sol® SD - 711 a powdered form of croscarmellose sodium, is utilized as a disintegrant and immediate release agent in pharmaceuticals and nutraceuticals. Its versatility is evident in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs), manufactured through wet granulation techniques.

IFF Pharma SolutionsPOLYOX™ WSR Coagulant 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 Coagulant LEO 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 SolutionsAvicel® CL - 611

Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
Dosage Form:Spray, Suspension
Labeling Claims:Triphenyl Tin Compounds-Free, Genotoxic-free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-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, Non-GMO, PAH-free, Not Tested on Animals, Tributyl Tin Compounds-Free, Odor-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, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Perfluorooctanoic Acid-free, Glycerin-free
Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), Kosher, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Japanese Pharmaceutical Excipients (JPE), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher
Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression

Avicel® CL - 611 a non-animal-origin ingredient, is used in sprays and suspensions. It's compatible with various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceuticals, it acts as a binder, filler, stabilizer, and immediate release agent. It's also an emulsifying agent and viscosity modifier, aiding suspension.

METHOCEL™ F4M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F4M Modified Cellulose Food Grade - Specialty

INCI Name:Methylcellulose
Ingredient Name:Hydroxypropyl Methyl Cellulose (HPMC)
Chemical Name:Hydroxypropyl Methylcellulose
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Vegetarian, Tributyl Tin Compounds-Free, Vegan, Low Odor, Non-GMO, Palm Oil-free, Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Mycotoxins-free, Kosher, Preservative-free, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Halal, Hypoallergenic, Hormones-free, PVC-free, Naturally Derived, Organic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, APE-free, Odor-free, Pesticide-free, Triphenyl Tin Compounds-Free, Generally Recognized As Safe (GRAS), CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Plasticizer-free, Dairy-free, VOC-free, Irradiation-free, TSE-free, Glycerin-free, Pareve, Sugar-free, PFOS-free, Perfluorooctanoic Acid-free, BSE-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Natural Latex Rubber-Free, Dioxin-free

METHOCEL™ F4M Modified Cellulose Food Grade - Specialty known for its water solubility, is utilized in various pharmaceutical and nutraceutical applications. It serves as a controlled release agent, film former, and gelling agent. Its manufacturing involves granulation and tablet coating processes.

IFF Pharma SolutionsMETHOCEL™ E3 Premium LV HPMC

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Tablets, Suspension
Ingredient Origin:Plant Origin
Labeling Claims:Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, Hypoallergenic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, VOC-free, TSE-free, Pareve, Perfluorooctanoic Acid-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, USP 232 Elemental Impurities Free, Mycotoxins-free, Kosher, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, APE-free, Odor-free, Pesticide-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan, Low Odor

METHOCEL™ E3 Premium LV HPMC suitable for suspensions, offers binding properties crucial for ceramic applications. With granulation and tablet coating manufacturing technologies, it ensures efficient production processes. Additionally, its water solubility makes it ideal for pharmaceutical and nutraceutical applications, serving as a binder and controlled release agent.

POLYOX™ WSR 301 NF Grade - Specialty banner

IFF Pharma SolutionsPOLYOX™ WSR 301 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 NF Grade - Specialty 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.

IFF Pharma SolutionsPOLYOX™ WSR - N12K NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - N12K NF Grade is an off-white powder with water-soluble properties. It's used as a binder and thickener in cleaning products and pharmaceuticals. Its applications include gels, osmotic pump tablets, and regular tablets, and it's manufactured using direct compression technology. Additionally, it serves as a controlled release agent.

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