Products

179 Products found on IFF Pharma Solutions

SDSWith SDS

TDSWith TDS

Chemical Name:Hydroxypropyl Starch, Carrageenan
Functions:Encapsulant
Labeling Claims:Hormones-free, Phthalates-free, Colorants-free, Paraben-free, Natural Latex Rubber-Free, Naturally Derived, Vegan, Halal, Triphenyl Tin Compounds-Free, Kosher, Non-GMO, PHO (Partially Hydrogenated Oil)-Free, Sustainable, Environmentally Friendly, Plasticizer-free, PAH-free, Pesticide-free, GMO-free, Palm Oil-free, Sugar-free, APE-free, Dye Free, PFAS-Free, Generally Recognized As Safe (GRAS), Vegetarian, Aluminum-free, Natural, Endocrine Disruptor-free, PVC-free, TSE-free, PFOS-free, Pareve, Perfluorooctanoic Acid-free, Preservative-free, Tributyl Tin Compounds-Free, Nitrosamines-free, BSE-free, Glycerin-free, Bisphenol A-free, Dioxin-free, Caffeine Free, Antibiotics-free, Animal Products-free, Monosodium Glutamate (MSG)-free
Certifications & Compliance:cGMP, Directive 1333/2008/EC, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, European Regulation 396/2005/EC, FSSC 22000, ISO 9001, Halal, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Doping-Free, IFANCA Halal, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, Regulation (EU) No. 1169/2011, Orthodox Union Kosher, EC No.1907/2006, Directive 396/2005/EC, FDA 21 CFR 177.1520, FDA 21 CFR 179.26, IFRA Compliant, Regulation (EU) No. 1272/2008
Dosage Form:Capsules

SeaGel® CAP - 202 ideal for capsules, utilizes encapsulation technology. It meets labeling claims like non-GMO, BSE-free, TSE-free, palm oil-free, glycerin-free, and endocrine disruptor-free, ensuring suitability for vegetarians. Its applications span food, nutrition, healthcare, and pharmaceuticals, serving in nutraceuticals, supplements, and oral drug delivery.

IFF Pharma SolutionsEndurance® VE - 102

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Functions:Binder
Manufacturing Technology:Direct Compression, Wet Granulation
Labeling Claims:Endocrine Disruptor-free, Natural Latex Rubber-Free, Dye Free, Kosher, Artificial Flavor-Free, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), Solvent-free, PAH-free, Allergen-free, Not Listed In California Proposition 65, Irradiation-free, Animal Products-free, Latex-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Not Tested on Animals, Perfluorooctanoic Acid-free, Palm Oil-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Ethylene Oxide-free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, Mercury-Free, BSE-free, Paraben-free, Halal, Non-GMO, GMO-free, Plasticizer-free, Zinc-free, Antibiotics-free, Pareve
Certifications & Compliance:Japan Pharmacopeia (JP), European Regulation 396/2005/EC, FSSC 22000, IFANCA Halal, Regulation (EU) No. 231/2012, ISO 45001, ISO 9001, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), Orthodox Union Kosher, United States Pharmacopeia (USP), ISO 14001, EC No.1907/2006, cGMP, FDA Food Safety Modernization Act (FSMA), ICH Q3C, Kosher, National Formulary (NF), Halal Food Council of Europe, Generally Recognized As Safe (GRAS), FCC Compliant, ISO 22000

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 SolutionsAc-Di-Sol® SD - 711

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Orally Disintegrating Tablets (ODTs), Capsules, Granules
Labeling Claims:Generally Recognized As Safe (GRAS), Vegan, Kosher, BSE-free, Non-GMO, Halal, TSE-free, Vegetarian, Pareve
Certifications & Compliance:EC No.1907/2006, Halal, Japan Pharmacopeia (JP), National Formulary (NF), FSSC 22000, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), IFANCA Halal, EXCiPACT, ISO 9001, Kosher
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.

METHOCEL™ F4M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F4M Modified Cellulose Food Grade - Specialty

INCI Name:Methylcellulose
Ingredient Name:Hydroxypropyl Methyl Cellulose (HPMC)
Chemical Name:Hydroxypropyl Methylcellulose
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Vegetarian, Tributyl Tin Compounds-Free, Vegan, Low Odor, Non-GMO, Palm Oil-free, Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Mycotoxins-free, Kosher, Preservative-free, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Halal, Hypoallergenic, Hormones-free, PVC-free, Naturally Derived, Organic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, APE-free, Odor-free, Pesticide-free, Triphenyl Tin Compounds-Free, Generally Recognized As Safe (GRAS), CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Plasticizer-free, Dairy-free, VOC-free, Irradiation-free, TSE-free, Glycerin-free, Pareve, Sugar-free, PFOS-free, Perfluorooctanoic Acid-free, BSE-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Natural Latex Rubber-Free, Dioxin-free

METHOCEL™ F4M Modified Cellulose Food Grade - Specialty known for its water solubility, is utilized in various pharmaceutical and nutraceutical applications. It serves as a controlled release agent, film former, and gelling agent. Its manufacturing involves granulation and tablet coating processes.

IFF Pharma SolutionsMETHOCEL™ E3 Premium LV HPMC

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Tablets, Suspension
Ingredient Origin:Plant Origin
Labeling Claims:Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, Hypoallergenic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, VOC-free, TSE-free, Pareve, Perfluorooctanoic Acid-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, USP 232 Elemental Impurities Free, Mycotoxins-free, Kosher, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, APE-free, Odor-free, Pesticide-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan, Low Odor

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 SolutionsAvicel® CL - 611

Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
Dosage Form:Spray, Suspension
Labeling Claims:Triphenyl Tin Compounds-Free, Genotoxic-free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Melamine-free, Colorants-free, Amine-free, Latex-free, Dioxin-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Not Tested on Animals, Tributyl Tin Compounds-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Perfluorooctanoic Acid-free, Glycerin-free
Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), Kosher, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Japanese Pharmaceutical Excipients (JPE), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher
Manufacturing Technology:Wet Granulation, Dry 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.

METHOCEL™ F50 Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F50 Modified Cellulose Food Grade - Specialty

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Hypoallergenic, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Odor-free, Phthalates-free, Dairy-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Non-GMO, Organic, Low Odor, Sewage Sludge Free, Plasticizer-free, Antibiotics-free, Pareve
Certifications & Compliance:Japan Pharmacopeia (JP), FDA 21 CFR 101.9, Swiss Ordinance (SR 817.023.21), JECFA (FAO/WHO), FEMA Compliant, European Regulation 396/2005/EC, FSSC 22000, 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, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Packaging Directive (94/62/EC), Orthodox Union Kosher, Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), FDA 21 CFR 172.874, Organic Certified, ISO 14001, FDA 21 CFR 175.105, ISO 50001, EC No.1907/2006, Indian Pharmacopeia, FDA 21 CFR 182.1480, FDA 21 CFR 176.180, cGMP, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, Halal, Quality Control BV Netherlands, FDA 21 CFR 176.170, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 2022/1396, FDA 21 CFR 175.300, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Regulation (EU) No. 1829/2003, FDA 21 CFR 174.5, Directive 2001/83/EC, Directive 2009/48/EC, REACH Exempt (Europe), British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, Regulation (EU) No. 1830/2003

METHOCEL™ F50 Modified Cellulose Food Grade - Specialty a modified cellulose of food grade, contains hypromellose and is manufactured using granulation and tablet coating technologies. It serves various functions in pharmaceuticals and nutraceuticals, including film formation, gelling, immediate and sustained release, as well as mucoadhesion and viscosity modification, thanks to its water-soluble nature.

IFF Pharma SolutionsPOLYOX™ WSR - N10 LEO NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - N10 LEO NF Grade an off-white powder, is prized for its water solubility, making it an effective binder and thickener in both cleaning and cosmetic products. Its versatility and solubility make it a valuable ingredient for various formulations.

IFF Pharma SolutionsProtanal® HF120 RBS

Chemical Name:Sodium Alginate
Labeling Claims:Halal, Paraben-free, Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP)
Chemical Inventories:PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China)

Protanal® HF120 RBS derived from non-animal sources, is potassium alginate, functioning as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceuticals and nutraceuticals. It is available in powder form.

IFF Pharma SolutionsProtanal® LF - MG 5/60

Chemical Name:Magnesium Alginate
Labeling Claims:Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free, Halal, Paraben-free
Certifications & Compliance:IFRA Compliant, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008
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 SolutionsMETHOCEL™ 254 HPMC - Specialty

INCI Name:Methylcellulose, Hydroxypropyl Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Phthalates-free, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Dairy-free, VOC-free, TSE-free, Pareve, Perfluorooctanoic Acid-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, Mycotoxins-free, Kosher, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, APE-free, Pesticide-free, Triphenyl Tin Compounds-Free, CMR Substances-free, Plasticizer-free, Irradiation-free, Glycerin-free, 1,4-Dioxane-free, Sugar-free, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan

METHOCEL™ 254 HPMC - Specialty sourced from plants, is recognized for its aluminum, antibiotics, APE, bisphenol A, and caffeine-free composition. It functions as a rheology modifier in industrial additives.

IFF Pharma SolutionsMETHOCEL™ K100M Premium HPMC

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Natural Latex Rubber-Free, Dioxin-free, Vegetarian, Tributyl Tin Compounds-Free, Vegan, Low Odor, Non-GMO, Palm Oil-free, Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, USP 232 Elemental Impurities Free, Mycotoxins-free, Kosher, Preservative-free, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Halal, Hypoallergenic, Hormones-free, PVC-free, Naturally Derived, Organic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, APE-free, Pesticide-free, Triphenyl Tin Compounds-Free, Generally Recognized As Safe (GRAS), CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Plasticizer-free, VOC-free, Irradiation-free, TSE-free, Glycerin-free, Pareve, Sugar-free, PFOS-free, Perfluorooctanoic Acid-free, BSE-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based

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.

IFF Pharma SolutionsETHOCEL™ Standard 14 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Controlled Release Agent, Granulation Aid, Binder, Taste Masker
Dosage Form:Tablets
Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, GMO-free, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), FDA 21 CFR 573.420, European Regulation 396/2005/EC, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, EC No. 1935/2004, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Encapsulation, Direct Compression

ETHOCEL™ Standard 14 Premium Ethylcellulose available in powder form, is adaptable for various manufacturing processes such as direct compression, encapsulation, and granulation. It exhibits ethanol solubility, offering versatility in pharmaceutical and industrial applications.

IFF Pharma SolutionsPOLYOX™ WSR - 303 LEO NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - 303 LEO NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.

IFF Pharma SolutionsPOLYOX™ WSR - 303 NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - 303 NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.

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