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16 Products found on IFF Pharma Solutions

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IFF Pharma SolutionsMETHOCEL™ E10M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose, Methylcellulose
CAS Number:9004-65-3
Dosage Form:Capsules, Suspension, Tablets
Labeling Claims:Low Odor, Odor-free, 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, 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, GMP, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA
Manufacturing Technology:Tablet Coating, Granulation, Wet Granulation

METHOCEL™ E10M Premium CR 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 SolutionsMETHOCEL™ A15C Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Dosage Form:Capsules, Tablets, Suspension
Labeling Claims:Low Odor, Tributyltin (TBT) - Free, Quaternary Ammonium Salt-Free, Dioxin-free, Phthalates-free, No Artificial Sweeteners, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, Natural Latex Rubber-Free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Herbicide-free, PFOA-free, Antibiotics-free, Palm Oil-free, PVC-free, Diethylene Glycol-free, PAH-free, Aluminum-free, NPE-free, Pesticide-free, Paraben-free, Potassium-free, Halal, Steroids Free, Bactericide-free, CMR Substances-free, Plasticizer-free, Ethylene Glycol-free, Bisphenol A-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Perfluorocarbon (PFC)-free, Sugar-free, Preservative-free, Glycerin-free, Artificial Flavor-Free, Vegetarian, FSSC 22000, APE-free, Hormones-free, PFOS-free, Naturally Derived, PFAS-Free, Impurities-free, Gluten-free, Fungicide-free, Low Aldehyde, Plant-Based, Radioactive-free
Certifications & Compliance:cGMP, Halal, FDA 21 CFR 172.874, 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.), FDA Food Safety Modernization Act (FSMA), Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), Directive 1333/2008/EC, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, GMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ A15C Premium Methylcellulose finds applications in suspension, tablet coating, and granulation for tablets and capsules. It is used in food containers and packaging. Features include being sewage-sludge-free. Functions as a controlled release agent, immediate release agent, thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive. It is water-soluble.

IFF Pharma SolutionsMETHOCEL™ VLV Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Orally Disintegrating Films (ODFs), Capsules, Granules, Suspension, Tablets
Labeling Claims:APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Naturally Derived, PFAS-Free, Impurities-free, Fungicide-free, PAH-free, Plant-Based, Radioactive-free, Potassium-free, Solvent-free, Low Odor, Odor-free, Quaternary Ammonium Salt-Free, Dioxin-free, Phthalates-free, No Artificial Sweeteners, Kosher, Colorants-free, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Residues-free, Persistent Organic Pollutants (POP)-free, 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, Non-Toxic, 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, FSSC 22000
Certifications & Compliance:Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, GMP, FDA 21 CFR 175.105, National Formulary (NF), European Parliament and Council Directive (E464), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA, FDA 21 CFR 176.180, Regulations (EU) No. 1129/2011, Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, SCF Listed, cGMP, Halal, REACH Exempt (Europe), British Pharmacopeia (BP), JECFA (FAO/WHO), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA 21 CFR 176.170, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EFSA (European Food Safety Authority) Certified, EXCiPACT, CFDA Compliant (China), FDA 21 CFR 175.300, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 1935/2004, FDA 21 CFR 174.5, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Directive 2012/19/EU, Regulation (EU) No. 1169/2011, FCC Compliant, EC No. 2023/2006, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Directive 2011/62/EU, Directive 1333/2008/EC
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.

IFF Pharma SolutionsSeaGel® CAP - 201

Chemical Name:Carrageenan
Functions:Encapsulant, Controlled Release Agent
Labeling Claims:Environmentally Friendly, Potassium-free, Dye Free, Plasticizer-free, PHO (Partially Hydrogenated Oil)-Free, Kosher, Paraben-free, PFAS-Free, Antibiotics-free, Aluminum-free, Plant-Based, Sustainable, Pesticide-free, PVC-free, Not Listed In California Proposition 65, Non-GMO, Vegetarian, Generally Recognized As Safe (GRAS), Iodide-free, Nitrosamines-free, Naturally Derived, Caffeine Free, Bisphenol Derivatives-free, Clean Label, Allergen-free, Fungicide-free, PFOS-free, Sugar-free, Hormones-free, Dioxane-free, Natural, APE-free, Natural Latex Rubber-Free, Quaternary Ammonium Salt-Free, Halal, Phthalates-free, Doping Substances-free, PFOA-free, BSE-free, Herbicide-free, Vegan, Preservative-free, Glycerin-free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Palm Oil-free, PAH-free, Gluten-free, Monosodium Glutamate (MSG)-free
Certifications & Compliance:Regulation (EU) No. 1272/2008, Clean Water Act (CWA) Certified, Nagoya Compliant
Dosage Form:Capsules

SeaGel® CAP - 201 identified as carrageenan, offers versatility and quality in capsule applications. With its natural and non-animal plant origins, it ensures ethical sourcing. Featuring easy-to-use powder form, it boasts film-forming properties, heat, and thermal stability. Additionally, it functions as an encapsulant and controlled release agent, providing enhanced performance in encapsulation processes.

IFF Pharma SolutionsAlubra® PG - 100

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

Alubra® PG - 100 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 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 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™ F50 Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Capsules, Suspension, Tablets
Labeling Claims:Low Odor, Quaternary Ammonium Salt-Free, BSE-free, Phthalates-free, Kosher, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dairy-free, Persistent Organic Pollutants (POP)-free, 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, Latex-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Fungicide-free, PAH-free, Iodide-free, Pareve, Potassium-free
Certifications & Compliance:cGMP, Halal, REACH Exempt (Europe), British Pharmacopeia (BP), Waste Electrical & Electronic Equipment Directive (WEEE), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA 21 CFR 176.170, FDA Food Safety Modernization Act (FSMA), Kosher, Swiss Ordinance (SR 817.023.21), EXCiPACT, FDA 21 CFR 175.300, United States Pharmacopeia (USP), FDA 21 CFR 174.5, Regulation (EU) No. 10/2011 (PIM), FSC Certified, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA Compliant, ICH Q3C, GMP, Nagoya Compliant, FDA 21 CFR 175.105, National Formulary (NF), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FDA 21 CFR 176.180, Belgian Law And Codex Alimentarius Standards
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ F50 Premium HPMC a cellulose ether also known as hypromellose, serves various functions across capsule, suspension, tablet, granulation, and tablet coating applications. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, thickener, and viscosity modifier. Notably, it is water-soluble, ensuring optimal formulation performance.

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 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.

IFF Pharma SolutionsAc-Di-Sol® SD - 711

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Capsules, Granules, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, 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, 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, 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:Halal, British Pharmacopeia (BP), China DMF, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, GMP, Nagoya Compliant, National Formulary (NF), FDA 21 CFR Regulations, Japan Pharmacopeia (JP)
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.

IFF Pharma SolutionsAquateric® N100

Dosage Form:Tablets, Capsules
Labeling Claims:Kosher, Non-GMO
Certifications & Compliance:Kosher

Aquateric® N100 available in powder form, is suitable for various dosage forms, such as capsules and tablets, particularly in dietary supplements. It serves as a release agent in food applications and offers the benefit of being non-GMO. Utilized in tablet coating manufacturing technology, it functions as an enteric coating system and an extended-release agent in pharmaceutical and nutraceutical products.

IFF Pharma SolutionsMETHOCEL™ K200M Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Capsules, Suspension, Tablets
Labeling Claims:Low Odor, Odor-free, Quaternary Ammonium Salt-Free, BSE-free, Phthalates-free, Kosher, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dairy-free, Persistent Organic Pollutants (POP)-free, 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, Latex-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Fungicide-free, PAH-free, Iodide-free, Pareve, Potassium-free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), Waste Electrical & Electronic Equipment Directive (WEEE), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA 21 CFR 176.170, FDA Food Safety Modernization Act (FSMA), Kosher, Swiss Ordinance (SR 817.023.21), EXCiPACT, FDA 21 CFR 175.300, United States Pharmacopeia (USP), FDA 21 CFR 174.5, Regulation (EU) No. 10/2011 (PIM), FSC Certified, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA Compliant, ICH Q3C, GMP, Nagoya Compliant, FDA 21 CFR 175.105, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FDA 21 CFR 176.180, Belgian Law And Codex Alimentarius Standards
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K200M Premium HPMC, identified as cellulose ethers and hypromellose, serves a wide array of functions across capsules, suspensions, tablets, granulation, and tablet coating applications. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, thickener, and viscosity modifier. Notably, it is water-soluble, ensuring versatility and efficacy in formulations.

IFF Pharma SolutionsAc-Di-Sol® SDW - 802

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Capsules, Granules, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Odor-free, Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, 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, 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, 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:Halal, British Pharmacopeia (BP), China DMF, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, Nagoya Compliant, National Formulary (NF), FDA 21 CFR Regulations, Japan Pharmacopeia (JP)
Manufacturing Technology:Wet Granulation

Ac-Di-Sol® SDW - 802 is a versatile ingredient suitable for capsules, granules, and orally disintegrating tablets (ODTs). Employing wet granulation, it serves as a disintegrant and immediate release agent in pharmaceutical and nutraceutical formulations.

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