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Pharmaceutical Actives & Precursors

202 Products found on IFF Pharma Solutions in Pharmaceuticals & Nutraceuticals

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TDSWith TDS

IFF Pharma SolutionsManucol® DH

Chemical Name:Sodium Alginate
Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Chemical Inventories:KECI (Korea), ENCS (Japan), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)

Manucol® DH cobalt, barium, and gold-free, functions as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, serving diverse roles in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsPOLYOX™ WSR - 301 LEO 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 - 301 LEO NF Grade 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 SolutionsSeaSpen® PF NF

Chemical Name:Trisodium orthophosphate, Calcium Sulfate, Carrageenan
Functions:Suspending Agent
Labeling Claims:Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Colorants-free, Triphenyl Tin Compounds-Free, Natural Latex Rubber-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Nitrosamines-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, APE-free, Caffeine Free, Dye Free, Preservative-free, PFAS-Free
Certifications & Compliance:EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Kosher, Doping-Free, FSSC 22000, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Regulation (EU) No. 231/2012, ISO 9001, IFRA Compliant
Dosage Form:Suspension

SeaSpen® PF NF in suspension form, adheres to various labeling claims including Kosher, Nitrosamines-free, GRAS, GMO-free, Non-GMO, and Palm Oil-free. It is utilized in oral drug delivery within the healthcare and pharmaceutical sectors, functioning as an excipient aiding in formulation and processing.

ETHOCEL™ Standard 20 TS Industrial Ethylcellulose - Specialty banner

IFF Pharma SolutionsETHOCEL™ Standard 20 TS Industrial Ethylcellulose - Specialty

Ingredient Name:Ethyl Cellulose
Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Chemical Family:Cellulose Ethers, Cellulose & Cellulosics
Pigment Type:Metallic Effect
Dosage Form:Tablets
Labeling Claims:Natural Latex Rubber-Free, Organic, Allergen-free, Dioxane-free, Antibiotics-free, Hormones-free, Dairy-free, Zero Calorie, Monosodium Glutamate (MSG)-free, Phthalates-free, Paraben-free, Non-Mutagenic, Non-Irritant, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, Aluminum-free, Sewage Sludge Free, Potassium-free, PFOA-free, PVC-free, Pesticide-free, FSSC 22000, Not Listed In California Proposition 65, Sugar-free, Iodide-free, 1,4-Dioxane-free, Nitrosamines-free, Gluten-free, Quaternary Ammonium Salt-Free, Plasticizer-free, Halal, PFOS-free, Bisphenol Derivatives-free, Caffeine Free, Irradiation-free, Odor-free, VOC-free, PFAS-Free, Kosher, Tributyltin (TBT) - Free, PAH-free
Color (Properties):White
Certifications & Compliance:Generally Recognized As Safe (GRAS), EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Directive 2012/19/EU, Regulation (EU) No. 1272/2008, Directive 2009/48/EC, Halal, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, FDA 21 CFR 73.1001, Japan Pharmacopeia (JP), FDA 21 CFR 101.9, National Formulary (NF), Chinese Pharmacopeia (ChP), ICH Q3C, EFSA (European Food Safety Authority) Certified, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, Belgian Law And Codex Alimentarius Standards, FDA 21 CFR 73.1, Kosher, ISO 9001, Organic Certified, Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), GMP, Directive 1333/2008/EC, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 117, FSSC 22000, United States Pharmacopeia (USP), FDA Compliant, EuPIA Listed, Regulation (EU) No. 231/2012, USDA Organic, Regulation (EC) No. 1333/2008, FSC Certified, JECFA (FAO/WHO), cGMP, FDA 21 CFR 172.868, RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), FDA Food Safety Modernization Act (FSMA)
Manufacturing Technology:Encapsulation, Granulation, Tablet Coating, Direct Compression

ETHOCEL™ Standard 20 TS Industrial Ethylcellulose - Specialty is ideal for granulation, tablet coating, and spray applications. It features good printability, reduced tack, and scuff resistance. This versatile component acts as a stabilizer, thickener, binder, and controlled release agent. Available in powder or granule form, its white color ensures compatibility with various industrial needs.

IFF Pharma SolutionsMETHOCEL™ E15 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Lubricant (Internal), Surfactant, Emulsifier, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Sustained Release Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Film Former, Solubilizer, Film Former
Dosage Form:Tablets, Suspension
Labeling Claims:Dye Free, Sewage Sludge Free, Odor-free, Triphenyl Tin Compounds-Free, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Mycotoxins-free, Pareve, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Aflatoxin-free, BSE-free, Palm Oil-free, Pesticide-free, Irradiation-free, Perfluorooctanoic Acid-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Allergen-free, Vegan, Hypoallergenic, Antibiotics-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, PVC-free, VOC-free
Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FSSC 22000, USDA Certified, Regulation (EU) No. 231/2012, ISO 9001, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, National Formulary (NF), Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, Kosher, European Regulation 396/2005/EC, ICH Q3C, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP)
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ E15 Premium LV HPMC is a water-soluble product used in granulation and tablet coating manufacturing. It serves as a binder in ceramics and pharmaceuticals, functioning as a binder, immediate release agent, mucoadhesive, solubilizer, and sustained release agent.

ETHOCEL™ Standard 4 Industrial Ethylcellulose - Specialty banner

IFF Pharma SolutionsETHOCEL™ Standard 4 Industrial Ethylcellulose - Specialty

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

ETHOCEL™ Standard 4 Industrial Ethylcellulose - Specialty is a white powder known for its solubility in organic solvents and ethanol. It offers benefits such as effective binding and controlled release, making it suitable for various industrial applications where these properties are essential.

IFF Pharma SolutionsGelcarin® PH - 379

Chemical Name:Carrageenan
CAS Number:9000-07-1
Labeling Claims:Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Allergen-free, Non-GMO, Paraben-free, Sugar-free, Aluminum-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Phthalates-free, Pesticide-free, PFOA-free, Kosher, Dioxane-free, Preservative-free, PFAS-Free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), Kosher, FDA 21 CFR 117, Halal, National Formulary (NF), Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), Nagoya Compliant, ABNT NBR 14725, FSSC 22000
Manufacturing Technology:Encapsulation

Gelcarin® PH - 379 is tailored for encapsulation, functioning as a controlled release agent, emulsifying agent, gelling agent, stabilizer, and thickener. Identified as a polysaccharide and specifically carrageenan, it ensures effective performance across diverse formulations.

IFF Pharma SolutionsAvicel® SMCC HD 90

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Zinc-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, Kosher, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, Regulation (EU) No. 1272/2008, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, British Pharmacopeia (BP), ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® SMCC HD 90 comprising non-animal origin microcrystalline cellulose, is utilized in various pharmaceutical and nutraceutical applications. Employing direct compression, dry granulation, and wet granulation manufacturing technologies, it serves as a compression aid, filler, and immediate release agent.

IFF Pharma SolutionsManucol® LMT

Chemical Name:Sodium Alginate
Labeling Claims:Not Listed In California Proposition 65, Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Chemical Inventories:TSCA (USA), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)

Manucol® LMT boasts a range of labeling claims, including being caffeine-free, colorant-free, dioxin-free, dye-free, hormone-free, and free of monosodium glutamate (MSG). In addition, it serves various functions in pharmaceuticals and nutraceuticals, acting as an antacid, controlled release agent, gelling agent, stabilizer, and thickener.

IFF Pharma SolutionsPOLYOX™ N60K LEO NF HV

Chemical Name:Polyethylene Oxide, Polyethylene Glycol, Pyrogenic Silica
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:Vegetarian, Residual Solvent -Free, Halal, Gluten-free, Non-GMO, Ethylene Oxide-free, Allergen-free, Vegan, Dairy-free, TSE-free, Herbicide-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, Fungicide-free, BSE-free, Not Tested on Animals, Pesticide-free, Diethylene Glycol-free, Irradiation-free, Chlorine-free, Doping Substances-free, VOC-free, Nitrosamines-free, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, ICH Q3C, EC No.1907/2006, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, 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), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), EXCiPACT, 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)

POLYOX™ N60K LEO NF HV containing polyethylene oxide (PEG-45M) serves multiple functions in various applications. Its versatility extends to deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. Functioning as a thickener, binder, and controlled release agent, it ensures optimal formulation performance. Available in powder form, it exhibits water solubility, enhancing its usability in diverse pharmaceutical formulations.

METHOCEL™ F450 Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F450 Modified Cellulose Food Grade - Specialty

Chemical Name:Hydroxypropyl Methylcellulose
Functions:Lubricant (Internal), Surfactant, Emulsifier, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Film Former
Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Organic, Hypoallergenic, Pareve, Residual Solvent -Free, APE-free, Plant-Based, PAH-free, Antibiotics-free, VOC-free, Paraben-free, Zero Calorie, Bisphenol A-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Tributyl Tin Compounds-Free, Low Odor, Kosher, PFAS-Free, Vegan, Dairy-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Mycotoxins-free, Caffeine Free, Dye Free, Monosodium Glutamate (MSG)-free, PFOS-free, Allergen-free, Irradiation-free, Non-GMO, Dioxin-free, Sugar-free, Aluminum-free, Triphenyl Tin Compounds-Free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Preservative-free
Certifications & Compliance:Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, GMP, Kosher, Halal, Doping-Free, ISO 9001, EU Directive 2002/72/EC, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Directive 2023/2055/EU, EU Cosmetic Regulation 1223/2009 Compliant, FFDCA, Organic Certified, Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, JECFA (FAO/WHO), ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, EC No. 1935/2004, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, United States Pharmacopeia (USP), FDA Compliant, REACH Exempt (Europe), ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, FDA 21 CFR 176.170, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, FCC Compliant, British Pharmacopeia (BP), FDA 21 CFR 176.180, cGMP, FDA 21 CFR 182.1480, EC No. 2023/2006, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, Regulation (EC) No. 1333/2008, EC No.1907/2006
Dosage Form:Tablets

METHOCEL™ F450 Modified Cellulose Food Grade - Specialty a modified cellulose with the chemical name Hypromellose, is utilized in various pharmaceutical and nutraceutical applications. Utilizing granulation and tablet coating manufacturing technologies, it serves as a binder, controlled release agent, film former, gelling agent, and immediate release agent, offering water solubility.

IFF Pharma SolutionsAvicel® DG

Chemical Name:Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Tablets
Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Ethylene Oxide-free, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Zinc-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, Kosher, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, Regulation (EU) No. 1272/2008, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® DG derived from non-animal sources, is a versatile powder used in tablet manufacturing. Its chemical composition includes calcium, hydrogen phosphate, cellulose, and cellulosics. Employing direct compression or wet granulation techniques, it functions as a binder and compression aid in tablet formulations.

IFF Pharma SolutionsMETHOCEL™ E4M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Lubricant (Internal), Surfactant, Emulsifier, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Sustained Release Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Thickener, Film Former, Solubilizer, Film Former
Dosage Form:Tablets, Suspension
Labeling Claims:Dye Free, Sewage Sludge Free, Odor-free, Triphenyl Tin Compounds-Free, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Mycotoxins-free, Pareve, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Aflatoxin-free, BSE-free, Palm Oil-free, Pesticide-free, Irradiation-free, Perfluorooctanoic Acid-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Allergen-free, Vegan, Not Listed In California Proposition 65, Hypoallergenic, Antibiotics-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, PVC-free, VOC-free
Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Directive 1333/2008/EC, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, National Formulary (NF), Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, European Regulation 396/2005/EC, ICH Q3C, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, FCC Compliant, USDA Organic, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP)
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ E4M Premium CR HPMC is water-soluble and used in suspensions, granulation, and tablet coating. It serves as a binder, controlled release agent, film former, gelling agent, and immediate release agent in pharmaceuticals and nutraceuticals, and as a binder in ceramics.

METHOCEL™ F50 Premium LV HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F50 Premium LV HPMC - Specialty

Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener, Binder, Emulsifier
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
End Uses:Ceramics
Dosage Form:Tablets
Certifications & Compliance:CFDA Compliant (China), Regulation (EC) No. 1333/2008, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Swiss Ordinance (SR 817.023.21), Organic Certified, FEMA Compliant, Chinese Pharmacopeia (ChP), WEEE Directive 2012/19/EU, Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), USDA Organic, Kosher, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, ICH Q3C, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, JECFA (FAO/WHO), EU Cosmetic Regulation 1223/2009 Compliant, British Pharmacopeia (BP), EXCiPACT, Doping-Free, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008, Directive 2023/915/EU, ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS)
Features:Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range

METHOCEL™ F50 Premium LV HPMC - Specialty serves as a versatile ingredient in various industries, functioning as a binder, controlled release agent, film former, gelling agent, immediate release agent, mucoadhesive, and solubilizer. Its water solubility makes it suitable for suspensions and various manufacturing processes.

IFF Pharma SolutionsMETHOCEL™ F50 Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Controlled Release Agent, Binder, Thickener, Mucoadhesive, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
Dosage Form:Capsules, Suspension, Tablets
Labeling Claims:PVC-free, Iodide-free, VOC-free, Nitrosamines-free, Persistent Organic Pollutants (POP)-free, PFAS-Free, Potassium-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, CMR Substances-free, Dye Free, Plasticizer-free, Sewage Sludge Free, APE-free, Quaternary Ammonium Salt-Free, Vegetarian, Halal, Tributyltin (TBT) - Free, Dioxane-free, USP 232 Elemental Impurities Free, Paraben-free, Gluten-free, PAH-free, PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Glycerin-free, Phthalates-free, Pareve, Allergen-free, Vegan, Dairy-free, PHO (Partially Hydrogenated Oil)-Free, Sugar-free, Antibiotics-free, Latex-free, TSE-free, Herbicide-free, Kosher, Ethylene Glycol-free, Fungicide-free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Bisphenol Derivatives-free, Organic, Diethylene Glycol-free, Irradiation-free
Certifications & Compliance:FDA 21 CFR 175.300, Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), REACH Exempt (Europe), FSC Certified, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), FDA 21 CFR 174.5, Waste Electrical & Electronic Equipment Directive (WEEE), Kosher, ICH Q3C, EC No.1907/2006, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, FDA 21 CFR 176.180, Directive 1333/2008/EC, Halal, FDA 21 CFR 172.874, FDA 21 CFR 175.105, European Pharmacopeia (Ph. Eur.), Nagoya Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, Orthodox Union Kosher, Indian Pharmacopeia, Swiss Ordinance (SR 817.023.21), Regulation (EU) No. 1169/2011, FDA 21 CFR 176.170, National Formulary (NF), USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ F50 Premium HPMC a cellulose ether also known as hypromellose, serves various functions across capsule, suspension, tablet, granulation, and tablet coating applications. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, thickener, and viscosity modifier. Notably, it is water-soluble, ensuring optimal formulation performance.

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