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143 Products found on IFF Pharma Solutions

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SeaGel® CAP - 202 banner
IFF Pharma SolutionsSeaGel® CAP - 202
  • Chemical Name:Hydroxypropyl Starch, Carrageenan
  • Functions:Encapsulant, Controlled Release Agent
  • Labeling Claims:Organic, Paraben-free, Phthalates-free, Tributyl Tin Compounds-Free, Triphenyl Tin Compounds-Free, Non-GMO, Dye Free, GMO-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Environmentally Friendly, Natural, Aluminum-free, PAH-free, TSE-free, Sustainable, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Palm Oil-free, Dioxin-free, APE-free, Preservative-free, Kosher, Bisphenol A-free, Sugar-free, Hormones-free, Naturally Derived, PFAS-Free, Vegetarian, Perfluorooctanoic Acid-free, Nitrosamines-free, Antibiotics-free, Animal Products-free, Plasticizer-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free
  • Certifications & Compliance:Directive 1333/2008/EC, Regulation (EU) No. 1829/2003, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, European Regulation 396/2005/EC, FSSC 22000, ISO 9001, cGMP, Halal, EU Cosmetic Regulation 1223/2009 Compliant, Doping-Free, Regulation (EU) No. 1272/2008, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1169/2011, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Directive 396/2005/EC, FDA 21 CFR 177.1520, Orthodox Union Kosher, FDA 21 CFR 179.26, IFRA Compliant
  • Dosage Form:Capsules
SeaGel® CAP - 202 ideal for capsules, utilizes encapsulation technology. It meets labeling claims like non-GMO, BSE-free, TSE-free, palm oil-free, glycerin-free, and endocrine disruptor-free, ensuring suitability for vegetarians. Its applications span food, nutrition, healthcare, and pharmaceuticals, serving in nutraceuticals, supplements, and oral drug delivery.
METHOCEL™ E3 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ E3 Premium LV HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Sustained Release Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Lubricant (Internal), Surfactant, Emulsifier, Binder, Thickener, Mucoadhesive, Immediate Release Agent, Film Former, 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, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Animal Products-free, 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), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FFDCA, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Halal, 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), Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ E3 Premium LV HPMC suitable for suspensions, offers binding properties crucial for ceramic applications. With granulation and tablet coating manufacturing technologies, it ensures efficient production processes. Additionally, its water solubility makes it ideal for pharmaceutical and nutraceutical applications, serving as a binder and controlled release agent.
Ac-Di-Sol® SD - 711 banner
IFF Pharma SolutionsAc-Di-Sol® SD - 711
  • Chemical Name:Croscarmellose Sodium
  • CAS Number:74811-65-7
  • Dosage Form:Orally Disintegrating Tablets (ODTs), Granules, Capsules
  • Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-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, USP 232 Elemental Impurities Free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR Regulations, FCC Compliant, British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, FSSC 22000, Orthodox Union Kosher, Regulation (EU) No. 1169/2011, IFANCA Halal, China DMF
  • Manufacturing Technology:Wet Granulation
Ac-Di-Sol® SD - 711 a powdered form of croscarmellose sodium, is utilized as a disintegrant and immediate release agent in pharmaceuticals and nutraceuticals. Its versatility is evident in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs), manufactured through wet granulation techniques.
Viscarin® PH - 209NF banner
IFF Pharma SolutionsViscarin® PH - 209NF
  • Chemical Name:Carrageenan
  • CAS Number:9000-07-1
  • Dosage Form:Soft Gels
  • Labeling Claims: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, Organic, APE-free, Caffeine Free, Dye Free, 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, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Vegan
  • Certifications & Compliance:FDA 21 CFR 177.1520, European Commission Decision 97/534/EC, European Pharmacopeia (Ph. Eur.), FDA 21 CFR 179.26, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FDA 7 CFR 205.605, ABNT NBR 14725, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, IFRA Compliant
  • Manufacturing Technology:Encapsulation
Viscarin® PH - 209NF utilizes encapsulation technology and is GMO-free, non-GMO, BSE-free, TSE-free, and palm oil-free. It caters to healthcare and pharma markets, particularly in oral drug delivery and care solutions. It serves as both an emulsifier and stabilizer and aids in formulation and processing in pharmaceutical and nutraceutical applications, including modified and controlled release formulations.
METHOCEL™ F4M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ F4M Modified Cellulose Food Grade - Specialty
  • Ingredient Name:Hydroxypropyl Methyl Cellulose (HPMC)
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Ingredient Origin:Plant Origin
  • Functions:Controlled Release Agent, Viscosity Modifier, Thickener, Film Former, Binder
  • Labeling Claims:Dye Free, Sewage Sludge Free, Odor-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Mycotoxins-free, Pareve, Dairy-free, 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, CMR Substances-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Vegan, Hypoallergenic, Antibiotics-free, TSE-free, Kosher, 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), FDA 21 CFR 174.5, JECFA (FAO/WHO), EC No. 2023/2006, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, Directive 1333/2008/EC, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, ISO 50001, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170, Regulation (EU) No. 1935/2004, National Formulary (NF), FDA 21 CFR 175.300, Directive 2001/83/EC, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, FDA 21 CFR 176.180, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, FDA 21 CFR 175.105, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), Directive 2023/2055/EU
  • Physical Form:Powder
  • Dosage Form:Tablets
METHOCEL™ F4M Modified Cellulose Food Grade - Specialty known for its water solubility, is utilized in various pharmaceutical and nutraceutical applications. It serves as a controlled release agent, film former, and gelling agent. Its manufacturing involves granulation and tablet coating processes.
SeaGel® CAP - 101 banner
IFF Pharma SolutionsSeaGel® CAP - 101
  • Chemical Name:Carrageenan
  • Functions:Encapsulant, Controlled Release Agent
  • Labeling Claims:Organic, Paraben-free, Phthalates-free, Tributyl Tin Compounds-Free, Triphenyl Tin Compounds-Free, Non-GMO, Dye Free, GMO-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Environmentally Friendly, Natural, Aluminum-free, PAH-free, TSE-free, Sustainable, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Palm Oil-free, Dioxin-free, APE-free, Preservative-free, Kosher, Bisphenol A-free, Sugar-free, Hormones-free, Naturally Derived, PFAS-Free, Vegetarian, Perfluorooctanoic Acid-free, Nitrosamines-free, Antibiotics-free, Animal Products-free, Plasticizer-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free
  • Certifications & Compliance:Directive 1333/2008/EC, Regulation (EU) No. 1829/2003, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, European Regulation 396/2005/EC, FSSC 22000, ISO 9001, cGMP, Halal, EU Cosmetic Regulation 1223/2009 Compliant, Doping-Free, Regulation (EU) No. 1272/2008, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1169/2011, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Directive 396/2005/EC, FDA 21 CFR 177.1520, Orthodox Union Kosher, FDA 21 CFR 179.26, IFRA Compliant
  • Dosage Form:Capsules
SeaGel® CAP - 101 ideal for capsules, utilizes encapsulation technology. It meets labeling claims like non-GMO, BSE-free, TSE-free, palm oil-free, glycerin-free, and endocrine disruptor-free, ensuring suitability for vegetarians. Its applications span food, nutrition, healthcare, and pharmaceuticals, serving in nutraceuticals, supplements, and oral drug delivery.
Protanal® LF - 240D banner
IFF Pharma SolutionsProtanal® LF - 240D
  • Chemical Name:Sodium Alginate
  • 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® LF - 240D sourced from non-animal origins, aligns with modern labeling preferences, being free from aluminum, antibiotics, and APE. Its multifunctionality in pharmaceuticals and nutraceuticals includes serving as an antacid, controlled release agent, gelling agent, stabilizer, and thickener, offering versatility in various applications.
METHOCEL™ A4M Premium Methylcellulose - Specialty banner
IFF Pharma SolutionsMETHOCEL™ A4M Premium Methylcellulose - Specialty
  • Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener
  • Chemical Name:Methylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • End Uses:Ceramics
  • Dosage Form:Tablets
  • Certifications & Compliance: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), EC No. 2023/2006, CFDA Compliant (China), Regulation (EC) No. 1333/2008, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, EC No. 1935/2004, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Organic Certified, Chinese Pharmacopeia (ChP), European Pharmacopeia (Ph. Eur.), USDA Organic, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, EU Directive 2002/72/EC, 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, 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
  • Features:Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range, Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties
METHOCEL™ A4M Premium Methylcellulose - Specialty a water-soluble additive, is utilized in granulation and wet granulation manufacturing. It functions as a binder in ceramics and pharmaceuticals, serving as a binder, film former, and gelling agent in various applications.
METHOCEL™ F50 Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ F50 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, REACH Exempt (Europe), 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™ F50 Modified Cellulose Food Grade - Specialty a modified cellulose of food grade, contains hypromellose and is manufactured using granulation and tablet coating technologies. It serves various functions in pharmaceuticals and nutraceuticals, including film formation, gelling, immediate and sustained release, as well as mucoadhesion and viscosity modification, thanks to its water-soluble nature.
METHOCEL™ K100M Premium HPMC banner
IFF Pharma SolutionsMETHOCEL™ K100M 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: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, 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™ K100M Premium HPMC is employed in ceramics as a binder, utilizing granulation in its manufacturing process. Within pharmaceuticals and nutraceuticals, it serves as a suspension aid, thickener, and viscosity modifier, boasting water solubility for versatile application.
Manucol® LMT2 banner
IFF Pharma SolutionsManucol® LMT2
  • Chemical Name:Sodium Alginate
  • Ingredient Name:Sodium Alginate
  • CAS Number:9005-38-3
  • Labeling Claims:Aluminum-free, Endocrine Disruptor-free, Dye Free, Plasticizer-free, Nanomaterials-free, Copper-free, Barium-free, APE-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, Cadmium-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, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, Cobalt-free, PVC-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Melamine-free, Gold-Free, PFAS-Free
  • Certifications & Compliance:Generally Recognized As Safe (GRAS), Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), EC No. 2023/2006, 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.), IFRA Compliant, EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EU) No. 1272/2008, Halal Food Council of Europe, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ABNT NBR 14725, ISO 9000, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP
  • Chemical Inventories:NDSL (Canada), ECL (Korea), PICCS (Phillipines), ENCS (Japan), IECSC (China), DSL (Canada), AICS (Australia)
Manucol® LMT2 is free from caffeine, colorants, dioxins, dyes, hormones, MSG, and natural latex rubber. It functions as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical formulations.
Manugel® DMB banner
IFF Pharma SolutionsManugel® DMB
  • Chemical Name:Sodium Alginate
  • 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, Gluten-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Formaldehyde-free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Gold-Free, Irradiation-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, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, Heavy Metal-free, PFAS-Free, Vegan
  • Certifications & Compliance: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, ISO 9001, United States Pharmacopeia (USP), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant
Manugel® DMB is free from copper, cobalt, barium, and gold. It serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications.
Avicel® CE-15 banner
IFF Pharma SolutionsAvicel® CE-15
  • Chemical Name:Guar Gum, Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
  • Dosage Form:Soft Chews, Tablets
  • Labeling Claims:Not Tested on Animals, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-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, TSE-free, Vegetarian, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, Kosher, Perchlorate-free, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Not Engineered With Nanomaterials, Preservative-free, PFAS-Free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, EC No. 1935/2004, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, EU Directive 2002/72/EC, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 10/2011 (PIM), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, FCC Compliant, British Pharmacopeia (BP), ISO 45001, Directive 1895/2005/EC, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, EC No. 2023/2006, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, IFANCA Halal, IFRA Compliant
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
Avicel® CE-15 a non-animal-derived ingredient, is widely employed in tablet production. It's adaptable to various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceutical and nutraceutical applications, it acts as a binder, compression aid, filler, immediate release agent, and suspension aid. It's supplied in powder form for easy tablet formulation.

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