Products

IFF Pharma Solutions

Matching Products Categories (6)

91 Products found on IFF Pharma Solutions

With SDS
With TDS
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.
Endurance® VE - 102 banner
IFF Pharma SolutionsEndurance® VE - 102
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Functions:Binder
  • Manufacturing Technology:Direct Compression, Wet Granulation
  • Labeling Claims:Dye Free, Plasticizer-free, APE-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Ethylene Oxide-free, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Solvent-free, Not Tested on Animals, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free, PFAS-Free, Zinc-free, Aluminum-free, Endocrine Disruptor-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Kosher, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), ISO 45001, ISO 14001, Orthodox Union Kosher, National Formulary (NF), FCC Compliant, ISO 22000, Generally Recognized As Safe (GRAS)
Endurance® VE - 102 comprising microcrystalline cellulose, finds applications in dietary supplements. It functions as a binder in food and nutrition, as well as in pharmaceuticals and nutraceuticals, presenting as a powder.
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.
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.
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® CR - 8133 banner
IFF Pharma SolutionsProtanal® CR - 8133
  • 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, Odor-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, 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), 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® CR - 8133 featuring sodium alginate, serves various functions in pharmaceuticals and nutraceuticals. It acts as an antacid, controlled release agent, emulsifying agent, gelling agent, thickener, and viscosity modifier, available in powder form.
Manucol® LD banner
IFF Pharma SolutionsManucol® LD
  • 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), 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® LD composed of sodium alginate, serves various pharmaceutical and nutraceutical functions, including antacid properties, controlled release, gelling, stabilization, and thickening.
METHOCEL™ VLV Premium HPMC banner
IFF Pharma SolutionsMETHOCEL™ VLV Premium HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Controlled Release Agent, Coating System, Binder, Thickener, Solubilizer, Film Former
  • Dosage Form:Capsules, Tablets, Suspension, Orally Disintegrating Films (ODFs), Granules
  • Labeling Claims:Sewage Sludge Free, Odor-free, Quaternary Ammonium Salt-Free, Halal, Tributyltin (TBT) - Free, USP 232 Elemental Impurities Free, Paraben-free, Gluten-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Perfluorocarbon (PFC)-free, Bisphenol A-free, Glycerin-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Herbicide-free, Palm Oil-free, Solvent-free, Pesticide-free, No Artificial Sweeteners, Low Aldehyde, Diethylene Glycol-free, Irradiation-free, Nitrosamines-free, PFAS-Free, Impurities-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, NPE-free, CMR Substances-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, FSSC 22000, Steroids Free, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Residues-free, Allergen-free, Vegan, Antibiotics-free, Radioactive-free, Kosher, Ethylene Glycol-free, Fungicide-free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Bactericide-free, Organic, Colorants-free, Plant-Based, PVC-free, Non-Toxic, VOC-free, Persistent Organic Pollutants (POP)-free, Potassium-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), FDA 21 CFR 174.5, JECFA (FAO/WHO), EC No. 2023/2006, SCF Listed, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Directive 1333/2008/EC, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, EU Cosmetic Regulation 1223/2009 Compliant, European Parliament and Council Directive (E464), FDA 21 CFR 176.170, Regulation (EU) No. 1935/2004, National Formulary (NF), FDA 21 CFR 175.300, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, Kosher, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, FDA 21 CFR 176.180, EC No. 1935/2004, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, FDA 21 CFR 175.105, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Directive 2012/19/EU, Regulation (EU) No. 1169/2011, FCC Compliant, Regulations (EU) No. 1129/2011, USDA Organic, EXCiPACT, Directive 2011/62/EU, EFSA (European Food Safety Authority) Certified, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), EU Directive 2002/72/EC, cGMP
  • Manufacturing Technology:Tablet Coating, Wet Granulation
METHOCEL™ VLV Premium HPMC is a versatile industrial additive designed for various applications, including tablet coating, orally disintegrating films, capsules, suspensions, and granules. With high efficiency and water solubility, it offers excellent cohesion development, green strength, and water retention. It functions as a binder, emulsifier, lubricant, and surfactant make it indispensable across manufacturing processes. Additionally, it serves as a water retention agent, binder and resin, slip agent, coating system, mucoadhesive, film former, viscosity modifier, solubilizer, gelling agent, and immediate release agent. METHOCEL™ VLV Premium HPMC's improved pumpability and lubricating properties ensure easy handling, making it a go-to choice for industrial and pharmaceutical formulations.
METHOCEL™ E50 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ E50 Premium LV HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Lubricant (Internal), Surfactant, Emulsifier, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Sustained Release Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Thickener, Film Former, Solubilizer, Film Former
  • Dosage Form:Tablets, Suspension
  • Labeling Claims:Dye Free, Sewage Sludge Free, Odor-free, Triphenyl Tin Compounds-Free, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Mycotoxins-free, Pareve, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Aflatoxin-free, BSE-free, Palm Oil-free, Pesticide-free, Irradiation-free, Perfluorooctanoic Acid-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Allergen-free, Vegan, Not Listed In California Proposition 65, Hypoallergenic, Antibiotics-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, PVC-free, VOC-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, National Formulary (NF), Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, European Regulation 396/2005/EC, ICH Q3C, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP)
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ E50 Premium LV HPMC is a versatile ingredient suitable for various applications. In suspension dosage forms, it serves as a binder for ceramics, while its granulation and tablet coating manufacturing technologies make it adaptable for different production processes. With properties such as film formation, gelling, and mucoadhesion, it functions in pharmaceutical and nutraceutical applications, facilitating immediate release and solubilization when needed.
Protanal® PH - 8133 banner
IFF Pharma SolutionsProtanal® PH - 8133
  • Chemical Name:Sodium Alginate
  • Ingredient Name:Sodium Alginate
  • CAS Number:9005-38-3
  • Labeling Claims:Gold-Free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Dye Free, Plasticizer-free, Nanomaterials-free, Copper-free, Barium-free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Residual Solvent -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, Solvent-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, Cobalt-free, PVC-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Melamine-free
  • Certifications & Compliance:GMP, Generally Recognized As Safe (GRAS), 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, Doping-Free, European Pharmacopeia (Ph. Eur.), IFRA Compliant, EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), ISO 14001, Regulation (EU) No. 1829/2003, Regulation (EU) No. 1272/2008, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ISO 9000, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP)
  • Chemical Inventories:NDSL (Canada), ECL (Korea), PICCS (Phillipines), ENCS (Japan), IECSC (China), DSL (Canada), AICS (Australia)
Protanal® PH - 8133 is a trusted choice, ensuring compliance with various labeling claims, including being non-GMO, solvent-free, and devoid of residual solvents, BSE, TSE, palm oil, mercury, copper, and cobalt. Its versatility extends to pharmaceutical applications, serving as emulsifiers, stabilizers, and aids in modified and controlled release formulations.
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.
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.

Show

of 91 results