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Pharmaceutical Actives & Precursors

169 Products found on IFF Pharma Solutions in Pharmaceuticals & Nutraceuticals

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IFF Pharma SolutionsProtacid® AR - 8640

Chemical Name:Alginic Acid
CAS Number:9005-32-7
Functions:Antacid, Controlled Release Agent
Labeling Claims:Dye Free, Plasticizer-free, Nanomaterials-free, APE-free, Triphenyl Tin Compounds-Free, Residual Solvent -Free, Halal, Paraben-free, Propylene Glycol-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Solvent-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Melamine-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free
Certifications & Compliance:Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), EC No. 2023/2006, Kosher, European Regulation 396/2005/EC, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, 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, ISO 14001, Regulation (EU) No. 1272/2008, Halal Food Council of Europe, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ISO 9000, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS)

Protacid® AR - 8640 belongs to the chemical family of alginates, specifically alginic acid. In pharmaceutical and nutraceutical applications, it serves as both an antacid and a controlled-release agent.

IFF Pharma SolutionsMETHOCEL™ F4M Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Controlled Release Agent, Suspending Agent, Binder, Thickener, Mucoadhesive, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
Dosage Form:Tablets
Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), REACH Exempt (Europe), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FSSC 22000, FDA Food Safety Modernization Act (FSMA), 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, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ F4M Premium HPMC 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.

IFF Pharma SolutionsETHOCEL™ Standard 100 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Controlled Release Agent, Binder, Granulation Aid, Taste Masker
Dosage Form:Tablets
Labeling Claims:PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, Paraben-free, PAH-free, PFOS-free, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, 1,4-Dioxane-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, Formaldehyde-free, PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free
Certifications & Compliance:Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Canadian Environmental Protection Act (CEPA), Kosher, European Regulation 396/2005/EC, ICH Q3C, Clean Air Act (CAA) Certified, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, EuPIA Listed, Halal, Directive 2023/915/EU, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 573.420, Regulation (EU) No. 10/2011 (PIM), Organic Certified, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, FDA 21 CFR 172.868, Regulation (EU) No. 1272/2008, FDA 21 CFR 73.1001, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, FCC Compliant, FDA 21 CFR 163, USDA Organic, EXCiPACT, FDA 21 CFR 73.1, Directive 2009/48/EC, British Pharmacopeia (BP)
Manufacturing Technology:Tablet Coating, Hot Melt Extrusion, Direct Compression, Granulation, Encapsulation

ETHOCEL™ Standard 100 Premium Ethylcellulose White powder for binding, controlled release, flexibility, and stability. It acts as a stabilizer and thickener in cosmetics, suitable for direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating. Soluble in ethanol and organic solvents.

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 SolutionsMETHOCEL™ K200M 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, Odor-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, Directive 2009/48/EC, British Pharmacopeia (BP), 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, 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, 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™ K200M Premium HPMC, identified as cellulose ethers and hypromellose, serves a wide array of functions across capsules, suspensions, tablets, 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 versatility and efficacy in formulations.

IFF Pharma SolutionsProtanal® LF - 200M

Chemical Name:Sodium Alginate
Labeling Claims:Steroids Free, Not Listed In California Proposition 65, No Artificial Sweeteners, Colorants-free, Copper-free, Natural Latex Rubber-Free, Naturally Derived, Halal, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, NPE-free, Pareve, Herbicide-free, Solvent-free, Perfluorocarbon (PFC)-free, Mycotoxins-free, Residual Solvent -Free, APE-free, Caffeine Free, Plant-Based, Barium-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Cobalt-free, Gold-Free, Irradiation-free, Non-GMO, 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, Cadmium-free, Palm Oil-free, Bactericide-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Radioactive-free, GMO-free, Kosher, Tin-free, 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, Kosher, FDA 21 CFR 117, Clean Water Act (CWA) Certified, Doping-Free, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 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), IFRA Compliant
Chemical Inventories:ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)

Protanal® LF- 200M is a versatile powder renowned for its role as a controlled release agent, gelling agent, thickener, stabilizer, and antacid in pharmaceutical and nutraceutical applications. Ensuring purity, it is swage-sludge-free, offering reliability in food ingredients.

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.

IFF Pharma SolutionsMETHOCEL™ K200M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Sustained Release Agent, Controlled Release Agent, Binder, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
Dosage Form:Suspension, Tablets
Labeling Claims:VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free
Certifications & Compliance:Directive 2009/48/EC, British Pharmacopeia (BP), National Bioengineered Food Disclosure Standard, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), 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, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K200M Premium CR HPMC used in ceramics and pharmaceuticals, acts as a binder and enables immediate release in suspensions and tablet coatings. It also serves as a film former, gelling agent, mucoadhesive, and solubilizer, offering versatile applications due to its water solubility.

IFF Pharma SolutionsManucol® LKX

Chemical Name:Sodium Alginate
Dosage Form:Tablets, Suspension
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, 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:ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)

Manucol® LKX serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications, available in both suspension and tablet forms.

IFF Pharma SolutionsPOLYOX™ WSR - 205 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:Vegetarian, Residual Solvent -Free, Halal, Gluten-free, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, 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, Chlorine-free, Doping Substances-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, 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)

POLYOX™ WSR - 205 FP NF Grade comprising ethylene oxide copolymers and polyethylene oxide (PEG-14M), serves multiple functions across various pharmaceutical applications. Its versatility extends to deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. Functioning as a binder and thickener, it ensures optimal formulation performance. Available in powder form, it exhibits water solubility, facilitating ease of use in pharmaceutical formulations.

IFF Pharma SolutionsMETHOCEL™ K100 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Sustained Release Agent, Controlled Release Agent, Binder, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
Dosage Form:Suspension, Tablets
Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), REACH Exempt (Europe), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K100 Premium LV HPMC is used in suspensions and as a binder in ceramics. It's manufactured using granulation and tablet coating processes. In pharmaceuticals and nutraceuticals, it serves as an immediate release agent and mucoadhesive due to its water-soluble nature.

IFF Pharma SolutionsPRONOVA® UP MVG

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Halal, Biodegradable
Certifications & Compliance:ISO 14001, National Formulary (NF), Hazard Analysis Critical Control Point (HACCP), European Pharmacopeia (Ph. Eur.), ISO 9000, United States Pharmacopeia (USP), GMP, Directive 2023/2055/EU, EC No.1907/2006
Manufacturing Technology:Encapsulation

PRONOVA® UP MVG is available in foam form with labeling claims of high purity and biodegradability. It contains sodium alginate, serves as an emulsifier and stabilizer, and is a is a modified and controlled release excipient. The product is supplied in solution form.

IFF Pharma SolutionsAvicel® SMCC - 50

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Tablets
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, 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, Halal Food Council of Europe, 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), 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 - 50 is used in tablet formulations, employing various manufacturing technologies like direct compression, dry granulation, and wet granulation. It serves multiple functions in pharmaceutical and nutraceutical applications, including acting as a binder, compression aid, filler, and immediate release agent.

IFF Pharma SolutionsAvicel® PH - 302

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Granules, Tablets, Suspension
Labeling Claims:Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Not Tested on Animals, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Genotoxic-free, Ethylene Glycol-free, Flavor Free, Melamine-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, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Kosher, Amine-free, Dioxane-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, 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), British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, cGMP, ABNT NBR 14725, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003, IFANCA Halal
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® PH - 302 identified as microcrystalline cellulose, is a cornerstone in pharmaceutical applications such as granules, suspensions, and tablets. Its versatility encompasses direct compression, dry granulation, and wet granulation processes. Functioning as a binder, compression aid, filler, and immediate release agent, Avicel® PH - 302 ensures robust formulations and consistent performance across diverse pharmaceutical products.

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