IFF Pharma Solutions

252 Products found on IFF Pharma Solutions in Excipients

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METHOCEL™ K15M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K15M Modified Cellulose Food Grade - Specialty

Chemical Name:Hydroxypropyl Methylcellulose
Functions:Controlled Release Agent
Labeling Claims:Dairy-free, Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Organic, Hypoallergenic, Pareve, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Plant-Based, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), VOC-free, Paraben-free, Dioxin-free, Zero Calorie, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, Low Odor, Kosher, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, JECFA (FAO/WHO), GMP, FEMA Compliant, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Swiss Ordinance (SR 817.023.21), Directive 1333/2008/EC, Directive 2023/2055/EU, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, FDA 21 CFR 176.180, FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), cGMP, FSSC 22000, FDA 21 CFR 182.1480, Orthodox Union Kosher, 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™ K15M Modified Cellulose Food Grade - Specialty known for its water solubility, is widely employed in granulation and tablet coating processes. Additionally, it serves as a controlled release agent and film former in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsMETHOCEL™ K100 HPMC - Specialty

Functions:Controlled Release Agent, Rheology Modifier
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Labeling Claims:Natural Latex Rubber-Free, Phthalates-free, Hormones-free, VOC-free, Generally Recognized As Safe (GRAS), TSE-free, Aflatoxin-free, Irradiation-free, PVC-free, Nitrosamines-free, 1,4-Dioxane-free, APE-free, Caffeine Free, Paraben-free, Vegan, PAH-free, Halal, Kosher, Mycotoxins-free, Sewage Sludge Free, CMR Substances-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Triphenyl Tin Compounds-Free, Naturally Derived, Sugar-free, Glycerin-free, Plant-Based, Dairy-free, Organic, Monosodium Glutamate (MSG)-free, Pesticide-free, Aluminum-free, Non-GMO, PFAS-Free, Vegetarian, Antibiotics-free, BSE-free, Bisphenol A-free, PFOS-free, Dye Free, Palm Oil-free, Preservative-free, Perfluorooctanoic Acid-free, Colorants-free, Plasticizer-free, Tributyl Tin Compounds-Free
Certifications & Compliance:European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), ISO 9001, RoHS 2 Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, FDA 21 CFR 182.1480, Regulation (EU) No. 1829/2003, EU Packaging Directive (94/62/EC), ISO 50001, USDA Organic, Turkish RoHS Regulation, Regulation (EC) No. 1333/2008, Halal, Directive 1333/2008/EC, Doping-Free, Directive 2009/48/EC, Majelis Ulama Indonesia Halal, Chinese Pharmacopeia (ChP), FDA Compliant, cGMP, ISO 14001, FSSC 22000, FDA 21 CFR 172.874, JECFA (FAO/WHO), European Pharmacopeia (Ph. Eur.), Swiss Ordinance (SR 817.023.21), WEEE Directive 2012/19/EU, Regulation (EU) No. 2022/1396, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2023/915/EU, Regulation (EU) No. 1830/2003, Regulation (EU) No. 231/2012, RoHS Compliant, FEMA Compliant, Kosher, FDA 21 CFR 101.9, Orthodox Union Kosher, Clean Air Act (CAA) Certified, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant
Dosage Form:Tablets

METHOCEL™ K100 HPMC - Specialty a cellulose ether derivative named Hypromellose, serves as a rheology modifier in industrial applications. Derived from plants, it exhibits water solubility, offering versatility in formulations.

IFF Pharma SolutionsPOLYOX™ WSR - N10 NF Grade

Chemical Name:Polyethylene Oxide, 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:Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, 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 - N10 NF Grade is an off-white powder with water-soluble properties. It's used as a binder and thickener in cleaning products and pharmaceuticals. Its applications include gels, osmotic pump tablets, and regular tablets, and it's manufactured using direct compression technology. Additionally, it serves as a controlled release agent.

IFF Pharma 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.

METHOCEL™ K100M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K100M Modified Cellulose Food Grade - Specialty

Chemical Name:Hydroxypropyl Methylcellulose
Functions:Controlled Release Agent
Labeling Claims:Dairy-free, Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Organic, Hypoallergenic, Pareve, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Plant-Based, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), VOC-free, Paraben-free, Dioxin-free, Zero Calorie, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, Low Odor, Kosher, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, JECFA (FAO/WHO), GMP, FEMA Compliant, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Swiss Ordinance (SR 817.023.21), Directive 1333/2008/EC, Directive 2023/2055/EU, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, FDA 21 CFR 176.180, FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), cGMP, FSSC 22000, FDA 21 CFR 182.1480, Orthodox Union Kosher, 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™ K100M Modified Cellulose Food Grade - Specialty known chemically as hypromellose, demonstrates water solubility and finds applications across various pharmaceutical and nutraceutical functions. It acts as a gelling agent, immediate release agent, mucoadhesive, solubilizer, sustained release agent, and viscosity modifier. Its versatility makes it suitable for use in granulation, tablet coating, and other formulation processes in the food industry.

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 SolutionsMETHOCEL™ K4M HPMC - Specialty

Functions:Controlled Release Agent, Rheology Modifier
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Labeling Claims:Persistent Organic Pollutants (POP)-free, Natural Latex Rubber-Free, Phthalates-free, Hormones-free, Bisphenol Derivatives-free, Herbicide-free, VOC-free, Dioxane-free, TSE-free, Aflatoxin-free, Irradiation-free, PVC-free, Nitrosamines-free, APE-free, Caffeine Free, Paraben-free, Vegan, Iodide-free, Latex-free, PAH-free, Halal, Kosher, Mycotoxins-free, Sewage Sludge Free, CMR Substances-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Sugar-free, Fungicide-free, PFOA-free, Diethylene Glycol-free, Allergen-free, Gluten-free, Glycerin-free, Dairy-free, Organic, Monosodium Glutamate (MSG)-free, Potassium-free, Pesticide-free, Aluminum-free, Non-GMO, PFAS-Free, Ethylene Glycol-free, Vegetarian, Antibiotics-free, BSE-free, Quaternary Ammonium Salt-Free, PFOS-free, Dye Free, Palm Oil-free, Preservative-free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 10/2011 (PIM), ISO 9001, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1169/2011, National Formulary (NF), GMP, Regulation (EU) No. 1829/2003, ISO 50001, Nagoya Compliant, FDA 21 CFR 174.5, USDA Organic, Regulation (EC) No. 1333/2008, Halal, Directive 1333/2008/EC, FDA 21 CFR 175.300, FDA 21 CFR 175.105, Directive 2009/48/EC, FDA 21 CFR 176.180, Chinese Pharmacopeia (ChP), FDA Compliant, cGMP, ISO 14001, FSSC 22000, FDA 21 CFR 172.874, Generally Recognized As Safe (GRAS), European Pharmacopeia (Ph. Eur.), Swiss Ordinance (SR 817.023.21), ICH Q3C, Regulation (EU) No. 2022/1396, Organic Certified, FDA Food Safety Modernization Act (FSMA), FSC Certified, Waste Electrical & Electronic Equipment Directive (WEEE), Regulation (EU) No. 1830/2003, Regulation (EU) No. 231/2012, Kosher, FDA 21 CFR 101.9, Orthodox Union Kosher, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170
Dosage Form:Tablets

METHOCEL™ K4M HPMC - Specialty, identified as cellulose ethers and hypromellose, serves as a rheology modifier, ensuring consistency in formulations. Notably, it is water-soluble, making it suitable for various applications.

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.

METHOCEL™ K15M Premium HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K15M Premium HPMC - Specialty

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

METHOCEL™ K15M Premium HPMC - Specialty with hypromellose as its chemical name, finds applications in ceramics as a binder. In pharmaceuticals and nutraceuticals, it serves as a gelling agent, mucoadhesive, solubilizer, suspension aid, thickener, and viscosity modifier, offering water solubility for various formulations.

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 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® 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.

IFF Pharma SolutionsProtanal® KF200 FTS

Chemical Name:Potassium Alginate
CAS Number:9005-36-1
Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -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, Vegetarian, TSE-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, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, 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), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant

Protanal® KF200 FTS derived from non-animal sources, is potassium alginate, functioning as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceuticals and nutraceuticals. It is available in powder form.

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.

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