Products

IFF Pharma Solutions

ExcipientsProduct Families

Modified & Controlled Release

Formulation & Processing Aids

Binders & Disintegrants

Emulsifiers & Stabilizers

Pharmaceutical Coatings

Solvents & Solubilizers

Other Excipients

Flavors & Taste Maskers

Fillers & Diluents

Base Fluids, Glidants & Lubricants

189 Products found on IFF Pharma Solutions in Excipients

SDSWith SDS

TDSWith TDS

IFF Pharma SolutionsAvicel® PH - 112

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Granules, Suspension, Tablets
Labeling Claims:Fragrance allergen-free, Quaternary Ammonium Salt-Free, BSE-free, Phthalates-free, Kosher, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, Herbicide-free, TSE-free, PFOA-free, Antibiotics-free, Bisphenol Derivatives-free, Palm Oil-free, Sugar-free, PVC-free, Diethylene Glycol-free, Gluten-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, CMR Substances-free, Dioxane-free, Plasticizer-free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Ethylene Oxide-free, Latex-free, APE-free, Hormones-free, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Fungicide-free, PAH-free, Iodide-free, Potassium-free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), ABNT NBR 14725, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA Compliant, ICH Q3C, FDA 21 CFR 117, Nagoya Compliant, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Belgian Law And Codex Alimentarius Standards
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

Avicel® PH - 112 is used in direct compression, dry granulation, and wet granulation applications. It is caffeine-free, CMR substance-free, diethylene glycol-free, and dioxane-free, ensuring safe and effective pharmaceutical formulations.

IFF Pharma SolutionsBD - 102

Chemical Name:Cellulose, Microcrystalline
Functions:Viscosity Modifier, Thickener
CAS Number:9004-34-6
Certifications & Compliance:National Formulary (NF)

BD - 102 serves as a thickener in pharmaceutical and nutraceutical formulations. Its main component is microcrystalline cellulose, aiding in various formulation and processing tasks.

IFF Pharma SolutionsSD - 600

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Labeling Claims:Odor-free
Certifications & Compliance:Regulation (EU) No. 1169/2011, National Formulary (NF), ICH Q3C, Japan Pharmacopeia (JP), ABNT NBR 14725, United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.)

SD - 600 belonging to the cellulose and cellulosics chemical family, features croscarmellose sodium as its chemical name. In pharmaceuticals and nutraceuticals, it functions as a thickener.

IFF Pharma SolutionsAlubra® PG - 30

Chemical Name:Sodium Stearyl Fumarate
CAS Number:4070-80-8
Dosage Form:Tablets
Labeling Claims:Plasticizer-free, Dioxin-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Phthalates-free, Preservative-free, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, Dye Free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Antibiotics-free, Sugar-free, PFAS-Free, PAH-free, PVC-free, Aluminum-free, Tributyl Tin Compounds-Free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free
Certifications & Compliance:FCC Compliant, REACH Exempt (Europe), British Pharmacopeia (BP), FDA Compliant, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), National Formulary (NF), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.)

Alubra® PG - 30 is available in both capsule and tablet forms, making it versatile for pharmaceutical applications. It meets labeling claims for being caffeine-free and free of colorants. In pharmaceutical and nutraceutical functions, it acts as an immediate release agent and a lubricant, aiding in the manufacturing process.

IFF Pharma SolutionsETHOCEL™ Medium 50 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, 1,4-Dioxane-free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, CMR Substances-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, Not Listed In California Proposition 65, PAH-free, Aflatoxin-free, Formaldehyde-free, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, Halal, British Pharmacopeia (BP), Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, RoHS Compliant, Swiss Ordinance (SR 817.023.21), EuPIA Listed, EXCiPACT, FDA 21 CFR 172.868, CFDA Compliant (China), RoHS 2 Compliant, Doping-Free, United States Pharmacopeia (USP), FDA 21 CFR 181.24, WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Japan Chemical Substances Control Law (CSCL), Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FCC Compliant, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, FDA 21 CFR 73.1001, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 573.420, ICH Q3C, Canadian Environmental Protection Act (CEPA), National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, ICH Q3D
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Direct Compression, Encapsulation

ETHOCEL™ Medium 50 Premium Ethylcellulose offers binding, controlled release, flexibility, and thermal stability. It serves as a stabilizer and thickener in cosmetics. Compatible with various manufacturing processes like direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating. It dissolves in organic solvents like ethanol and isopropanol.

IFF Pharma SolutionsMETHOCEL™ E3 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Suspension
Labeling Claims:Low Odor, Odor-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:Halal, British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, Regulation (EU) No. 2022/1396, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS)
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.

IFF Pharma SolutionsProtanal® LF - 200FTS

Chemical Name:Sodium Alginate
Labeling Claims:Tin-free, Quaternary Ammonium Salt-Free, Dioxin-free, BSE-free, Gold-Free, Phthalates-free, No Artificial Sweeteners, Cadmium-free, Kosher, Colorants-free, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Herbicide-free, TSE-free, PFOA-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Gluten-free, Aluminum-free, NPE-free, Pesticide-free, Steroids Free, Paraben-free, Bactericide-free, CMR Substances-free, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Perfluorocarbon (PFC)-free, Preservative-free, Glycerin-free, Artificial Flavor-Free, Vegetarian, Bisphenol A-free, Barium-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Impurities-free, Fungicide-free, PAH-free, Radioactive-free, Mercury-Free, Potassium-free, Residual Solvent -Free, Cobalt-free, Solvent-free
Certifications & Compliance:cGMP, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 117, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA
Chemical Inventories:PICCS (Phillipines), AICS (Australia), ENCS (Japan), IECSC (China), NDSL (Canada), DSL (Canada), ECL (Korea)

Protanal® LF- 200FTS is a versatile powder designed for various applications in food ingredients, pharmaceuticals, and nutraceuticals. This product boasts features like being sewage-sludge-free, ensuring purity and safety. It functions as a controlled release agent, gelling agent, thickener, and stabilizer, offering multifunctionality. In pharmaceuticals and nutraceuticals, it also serves as an antacid, providing added value.

IFF Pharma SolutionsViscarin® PH - 109NF

Chemical Name:Carrageenan
CAS Number:9000-07-1
Dosage Form:Soft Gels
Labeling Claims:Triphenyl Tin Compounds-Free, Plasticizer-free, Dioxin-free, Monosodium Glutamate (MSG)-free, BSE-free, Generally Recognized As Safe (GRAS), Caffeine Free, Phthalates-free, Preservative-free, Colorants-free, Glycerin-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegetarian, Bisphenol A-free, Vegan, APE-free, Hormones-free, Dye Free, GMO-free, Natural Latex Rubber-Free, TSE-free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Antibiotics-free, Palm Oil-free, Sugar-free, Non-GMO, PFAS-Free, PAH-free, PVC-free, Aluminum-free, Tributyl Tin Compounds-Free, Pesticide-free, Paraben-free
Certifications & Compliance:Regulation (EU) No. 1169/2011, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, ABNT NBR 14725, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Regulation (EU) No. 231/2012, Doping-Free, European Regulation 396/2005/EC, National Formulary (NF), European Pharmacopeia (Ph. Eur.)
Manufacturing Technology:Encapsulation

Viscarin® PH - 109NF employing encapsulation technology, offers BSE-free, TSE-free, palm oil-free, and glycerin-free formulations. It serves as a controlled release agent, encapsulant, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsAccelerate® DS - 813

Chemical Name:Cellulose Gum
Functions:Disintegrant
Manufacturing Technology:Wet Granulation
Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Vegan, Dye Free, Pesticide-free, GMO-free, Allergen-free, Aluminum-free, Generally Recognized As Safe (GRAS), Natural Latex Rubber-Free, PFAS-Free, Preservative-free, PFOS-free, Nanomaterials-free, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Not Listed In California Proposition 65, Palm Oil-free, Hormones-free, Melamine-free, Endocrine Disruptor-free, Sugar-free, Tributyl Tin Compounds-Free, Antibiotics-free, Glycerin-free, BSE-free, PVC-free, PAH-free, Phthalates-free, Triphenyl Tin Compounds-Free, Caffeine Free, TSE-free, Plasticizer-free, APE-free, Ethylene Oxide-free, Non-GMO, Vegetarian
Certifications & Compliance:Regulation (EU) No. 231/2012, ICH Q3C, European Pharmacopeia (Ph. Eur.), Nagoya Compliant, FDA 21 CFR Regulations, FDA Food Safety Modernization Act (FSMA), United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, cGMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), European Regulation 396/2005/EC, Doping-Free

Accelerate® DS - 813 is available in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs). Manufactured using wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical formulations. It is supplied in powder form for ease of processing and formulation.

IFF Pharma SolutionsSeaSpen® PF NF

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

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

IFF Pharma SolutionsProtanal® PH - 1033

Chemical Name:Sodium Alginate
Labeling Claims:Tin-free, Quaternary Ammonium Salt-Free, Dioxin-free, BSE-free, Gold-Free, Phthalates-free, No Artificial Sweeteners, Cadmium-free, Kosher, Colorants-free, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Herbicide-free, TSE-free, PFOA-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Gluten-free, Aluminum-free, NPE-free, Pesticide-free, Steroids Free, Paraben-free, Bactericide-free, CMR Substances-free, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Perfluorocarbon (PFC)-free, Preservative-free, Glycerin-free, Artificial Flavor-Free, Vegetarian, Bisphenol A-free, Barium-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Impurities-free, Fungicide-free, PAH-free, Radioactive-free, Mercury-Free, Potassium-free, Residual Solvent -Free, Cobalt-free, Solvent-free
Certifications & Compliance:cGMP, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 117, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA
Chemical Inventories:PICCS (Phillipines), AICS (Australia), ENCS (Japan), IECSC (China), NDSL (Canada), DSL (Canada)

Protanal® PH - 1033 is a versatile powder free from sewage sludge. Ideal for pharmaceuticals and nutraceuticals, it serves as a controlled release agent, gelling agent, thickener, and stabilizer. Plus, it offers antacid properties, ensuring top-notch performance in various applications.

IFF Pharma SolutionsProtanal® LF - MG 5/60

Chemical Name:Magnesium Alginate
Labeling Claims:Dioxin-free, BSE-free, Gold-Free, Phthalates-free, Cadmium-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Barium-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Residual Solvent -Free, Cobalt-free, Solvent-free
Certifications & Compliance:Halal, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Japan Pharmacopeia (JP)
Chemical Inventories:AICS (Australia), NDSL (Canada), DSL (Canada)

Protanal® LF - MG 5/60 is a non-animal origin powder serving multiple functions in pharmaceuticals and nutraceuticals. It acts as an antacid, controlled release agent, gelling agent, and stabilizer, providing versatile benefits for various formulations.

IFF Pharma SolutionsPRONOVA® UP VLVM

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
Manufacturing Technology:Encapsulation

PRONOVA® UP VLVM 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 SolutionsPRONOVA® UP MVM

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
Manufacturing Technology:Encapsulation

PRONOVA® UP MVM 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 SolutionsCELSENTIAL™ E5 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
Functions:Viscosity Modifier
CAS Number:9004-65-3
Labeling Claims:CMR Substances-free, Odor-free, BSE-free, TSE-free, Kosher, Endocrine Disruptor-free
Certifications & Compliance:Turkish RoHS Regulation, ICH Q3C, REACH Exempt (Europe), GMP, United States Pharmacopeia (USP), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), Kosher

CELSENTIAL™ E5 Premium LV HPMC, a cellulose ether known as hypromellose, adeptly modifies viscosity. It's certified BSE-free and CMR substance-free, guaranteeing safety and adherence to strict regulatory standards.

Show

of 189 results