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92 Products found on IFF Pharma Solutions

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IFF Pharma SolutionsMETHOCEL™ E6 Premium LV Capsule Grade HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Capsules, Suspension, Tablets
Labeling Claims:Low Odor, Quaternary Ammonium Salt-Free, Dioxin-free, Phthalates-free, No Artificial Sweeteners, Colorants-free, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Herbicide-free, PFOA-free, Antibiotics-free, Palm Oil-free, Sugar-free, Low Aldehyde, PVC-free, Diethylene Glycol-free, Gluten-free, Aluminum-free, NPE-free, Pesticide-free, Steroids Free, Paraben-free, Halal, Bactericide-free, CMR Substances-free, Plasticizer-free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Perfluorocarbon (PFC)-free, Preservative-free, Glycerin-free, Artificial Flavor-Free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Hypoallergenic, PFOS-free, Naturally Derived, PFAS-Free, Impurities-free, Fungicide-free, PAH-free, Plant-Based, Radioactive-free, Potassium-free
Certifications & Compliance:Halal, REACH Exempt (Europe), British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), 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, Regulation (EC) No. 1333/2008, FDA Compliant, Directive 1333/2008/EC, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, Regulation (EU) No. 2022/1396, GMP, National Formulary (NF), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA
Manufacturing Technology:Tablet Coating, Granulation, Wet Granulation

METHOCEL™ E6 Premium LV Capsule Grade HPMC is a versatile product with various applications and functions. Ideal for tablet coating, granulation, wet granulation, tablets, and capsules, it ensures controlled and immediate release. Free from sewage sludge, it serves as a thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive, making it indispensable in pharmaceutical and nutraceutical formulations. Suitable for food containers and packaging, it boasts water solubility, ensuring quality performance in suspension formulations.

IFF Pharma SolutionsGelcarin® GP - 379

Chemical Name:Carrageenan
CAS Number:9000-07-1
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-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.), Regulation (EU) No. 1169/2011, FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Japan Pharmacopeia (JP)
Manufacturing Technology:Encapsulation

Gelcarin® GP - 379 derived from carrageenan of non-animal origin, serves various pharmacological and nutraceutical functions, including being a controlled-release agent, emulsifying agent, gelling agent, stabilizer, and thickener.

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 SolutionsEndurance® VE - 102

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Functions:Binder
Manufacturing Technology:Wet Granulation, Direct Compression
Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Dye Free, Pesticide-free, GMO-free, Allergen-free, Aluminum-free, Generally Recognized As Safe (GRAS), Natural Latex Rubber-Free, Kosher, PFAS-Free, Preservative-free, PFOS-free, Halal, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Palm Oil-free, Hormones-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, Latex-free, Non-GMO
Certifications & Compliance:Regulation (EU) No. 231/2012, ICH Q3C, European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), National Formulary (NF), United States Pharmacopeia (USP), cGMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FCC Compliant, European Regulation 396/2005/EC, Halal, Doping-Free

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.

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 SolutionsMETHOCEL™ K100 Premium LVCR 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, CMR Substances-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), 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:cGMP, Halal, EU Packaging Directive (94/62/EC), British Pharmacopeia (BP), JECFA (FAO/WHO), ABNT NBR 14725, FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, Swiss Ordinance (SR 817.023.21), EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, FEMA Compliant, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, 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), Directive 2023/915/EU
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K100 Premium LVCR HPMC belonging to the cellulose ether chemical family, is manufactured using granulation technology. In pharmaceuticals and nutraceuticals, it serves as a controlled release agent, film former, gelling agent, immediate release agent, and mucoadhesive, offering water solubility for diverse applications.

IFF Pharma SolutionsManugel® DMB

Chemical Name:Sodium Alginate
Labeling Claims:Melamine-free, Dioxin-free, BSE-free, Gold-Free, Phthalates-free, Cadmium-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-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, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Irradiation-free, Glycerin-free, Vegetarian, Bisphenol A-free, Barium-free, Latex-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, Heavy Metal-free, PFAS-Free, PAH-free, Aflatoxin-free, Formaldehyde-free, Tributyl Tin Compounds-Free, Mercury-Free, Residual Solvent -Free, Cobalt-free
Certifications & Compliance:FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, Doping-Free, European Regulation 396/2005/EC, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Generally Recognized As Safe (GRAS)

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.

IFF Pharma SolutionsSeaGel® CAP - 101

Chemical Name:Carrageenan
Functions:Encapsulant, Controlled Release Agent
Labeling Claims:Monosodium Glutamate (MSG)-free, GMO-free, Environmentally Friendly, Dye Free, Colorants-free, Plasticizer-free, PHO (Partially Hydrogenated Oil)-Free, Kosher, Paraben-free, PFAS-Free, Antibiotics-free, Perfluorooctanoic Acid-free, Tributyl Tin Compounds-Free, Bisphenol A-free, Aluminum-free, Sustainable, Pesticide-free, PVC-free, Non-GMO, Vegetarian, Generally Recognized As Safe (GRAS), Nitrosamines-free, Naturally Derived, Caffeine Free, PFOS-free, Sugar-free, Hormones-free, Natural, APE-free, Natural Latex Rubber-Free, Halal, Phthalates-free, BSE-free, Vegan, Preservative-free, Glycerin-free, Triphenyl Tin Compounds-Free, Endocrine Disruptor-free, TSE-free, Palm Oil-free, PAH-free, Dioxin-free
Certifications & Compliance:IFRA Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Doping-Free, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Halal, Regulation (EU) No. 231/2012, EU Cosmetic Regulation 1223/2009 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.

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 SolutionsMETHOCEL™ A4M Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
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, Nitrosamines-free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, Not Listed In California Proposition 65, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, 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, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP)
Manufacturing Technology:Granulation, Wet Granulation

METHOCEL™ A4M Premium Methylcellulose 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.

IFF Pharma SolutionsAccelerate® DS - 812

Chemical Name:Cellulose Gum, Croscarmellose Sodium
Dosage Form:Capsules, Granules, Tablets, Soft Chews, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Odor-free, Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Colorants-free, Nanomaterials-free, Endocrine Disruptor-free, Allergen-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, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, Nagoya Compliant, FDA 21 CFR Regulations
Manufacturing Technology:Wet Granulation

Accelerate® DS - 812 contains cellulose gum and is available in capsule, granule, and orally disintegrating tablet forms. Utilizing wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsViscarin® PH - 209NF

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, Not Listed In California Proposition 65, 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 - 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.

IFF Pharma SolutionsMETHOCEL™ E15 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:USDA Certified, Halal, British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, 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™ E15 Premium LV HPMC is a water-soluble product used in granulation and tablet coating manufacturing. It serves as a binder in ceramics and pharmaceuticals, functioning as a binder, immediate release agent, mucoadhesive, solubilizer, and sustained release agent.

IFF Pharma SolutionsAvicel® CL - 611

Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
Dosage Form:Suspension, Spray
Labeling Claims:Odor-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Allergen-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, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, Latex-free, APE-free, Hormones-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Japanese Pharmaceutical Excipients (JPE), United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, GMP, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS)
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

Avicel® CL - 611 a non-animal-origin ingredient, is used in sprays and suspensions. It's compatible with various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceuticals, it acts as a binder, filler, stabilizer, and immediate release agent. It's also an emulsifying agent and viscosity modifier, aiding suspension.

IFF Pharma SolutionsSeaGel® CAP 203

Chemical Name:Carrageenan, Hydroxypropyl Starch
Functions:Encapsulant, Controlled Release Agent
Labeling Claims:Monosodium Glutamate (MSG)-free, GMO-free, Environmentally Friendly, Dye Free, Colorants-free, Plasticizer-free, PHO (Partially Hydrogenated Oil)-Free, Kosher, Paraben-free, PFAS-Free, Antibiotics-free, Perfluorooctanoic Acid-free, Tributyl Tin Compounds-Free, Bisphenol A-free, Aluminum-free, Sustainable, Pesticide-free, PVC-free, Non-GMO, Vegetarian, Generally Recognized As Safe (GRAS), Nitrosamines-free, Naturally Derived, Caffeine Free, PFOS-free, Sugar-free, Hormones-free, Natural, APE-free, Natural Latex Rubber-Free, Halal, Phthalates-free, BSE-free, Vegan, Preservative-free, Glycerin-free, Triphenyl Tin Compounds-Free, Endocrine Disruptor-free, TSE-free, Palm Oil-free, PAH-free, Dioxin-free
Certifications & Compliance:IFRA Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Doping-Free, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Halal, Regulation (EU) No. 231/2012, EU Cosmetic Regulation 1223/2009 Compliant
Dosage Form:Capsules

SeaGel® CAP 203 consisting of Hydroxypropyl Starch, is primarily designed for capsule applications. It boasts food ingredient features such as being easy to use, film-forming, heat-stable, high-quality, and pH neutral, all in a convenient powder form.

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