Certifications Compliance Chinese Pharmacopoeia Chp - Excipients - Pharmaceuticals & Nutraceuticals - IFF Pharma Solutions - page 2

173 Products found on IFF Pharma Solutions in Excipients

SDSWith SDS

TDSWith TDS

Chemical Name:Sodium Alginate
Ingredient Name:Sodium Alginate
CAS Number:9005-38-3
Labeling Claims:Antibiotics-free, Pareve, Copper-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Dye Free, Kosher, Cobalt-free, Propylene Glycol-free, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), PAH-free, Allergen-free, Irradiation-free, Animal Products-free, Melamine-free, Latex-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, Barium-free, Mycotoxins-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, Cadmium-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, Mercury-Free, Gold-Free, BSE-free, Paraben-free, Halal, Non-GMO, GMO-free, Nanomaterials-free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, European Pharmacopeia (Ph. Eur.), IFRA Compliant, EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, National Formulary (NF), Halal Food Council of Europe, EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, ABNT NBR 14725, ISO 9000, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
Chemical Inventories:NDSL (Canada), IECSC (China), PICCS (Phillipines), DSL (Canada), ECL (Korea), AICS (Australia), ENCS (Japan)

Manucol® LMT2 is free from caffeine, colorants, dioxins, dyes, hormones, MSG, and natural latex rubber. It functions as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical formulations.

ETHOCEL™ Standard 7 LT Industrial Ethylcellulose - Specialty banner

IFF Pharma SolutionsETHOCEL™ Standard 7 LT Industrial Ethylcellulose - Specialty

Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Pigment Type:Metallic Effect
Dosage Form:Tablets
Labeling Claims:Caffeine Free, Organic, Irradiation-free, VOC-free, Quaternary Ammonium Salt-Free, PFOS-free, Dioxane-free, Dairy-free, Odor-free, Tributyltin (TBT) - Free, Allergen-free, Natural Latex Rubber-Free, Zero Calorie, Nitrosamines-free, Bisphenol Derivatives-free, Pesticide-free, Non-GMO, Kosher, Hormones-free, APE-free, Sugar-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, FSSC 22000, PHO (Partially Hydrogenated Oil)-Free, Iodide-free, Gluten-free, Sewage Sludge Free, Paraben-free, Phthalates-free, Dye Free, 1,4-Dioxane-free, PAH-free, Halal, Preservative-free, PVC-free, Potassium-free, PFOA-free, Aluminum-free, PFAS-Free, Antibiotics-free, Non-Irritant, Non-Mutagenic
Color (Properties):White
Certifications & Compliance:FDA 21 CFR 101.9, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, ISO 9001, Organic Certified, cGMP, GMP, Directive 1333/2008/EC, ICH Q3C, Directive 2011/65/EU (RoHS 2), FSSC 22000, United States Pharmacopeia (USP), EFSA (European Food Safety Authority) Certified, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 172.868, FSC Certified, FDA Food Safety Modernization Act (FSMA), JECFA (FAO/WHO), RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), EuPIA Listed, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Regulation (EU) No. 1272/2008, Directive 2012/19/EU, Directive 2009/48/EC, Halal, USDA Organic, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), Kosher, FDA 21 CFR 117, Chinese Pharmacopeia (ChP), EC No.1907/2006
Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation

ETHOCEL™ Standard 7 LT Industrial Ethylcellulose - Specialty is suitable for spray, phenolics, modified rosins, and alkyds (Long Oil) applications. It features high gloss, good printability, and reduced tack, ensuring quality finishes. Acting as a rheology modifier, binder & resin, and stabilizer, it's available in powder or granule form, presenting a white color for versatility in industrial processes.

IFF Pharma SolutionsPOLYOX™ WSR - N60K SFP 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 - N60K SFP NF Grade an off-white powder, offers versatile applications. Its industrial additives function as binders and thickeners, aiding in direct compression manufacturing. In pharmaceuticals, it acts as a binder and controlled release agent. Soluble in water, it suits abuse deterrent tablets & capsules, gels, and osmotic pump tablets.

IFF Pharma SolutionsPOLYOX™ WSR - N80 FP 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 - N80 FP NF Grade with its off-white color and powder form, exhibits versatile applications. In cosmetics, it functions as both a binder and a thickener, while in industrial additives, it serves similar purposes, offering water solubility for ease of use across various formulations.

IFF Pharma SolutionsMETHOCEL™ F50 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, Halal, Hypoallergenic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, Generally Recognized As Safe (GRAS), 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, CMR Substances-free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, Not Listed In California Proposition 65, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan, Low Odor

METHOCEL™ F50 Premium LV HPMC serves as a versatile ingredient in various industries, functioning as a binder, controlled release agent, film former, gelling agent, immediate release agent, mucoadhesive, and solubilizer. Its water solubility makes it suitable for suspensions and various manufacturing processes.

METHOCEL™ K200M Premium HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K200M Premium HPMC - Specialty

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
Labeling Claims:Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, Potassium-free, PAH-free, Caffeine Free, Sewage Sludge Free, Herbicide-free, PFOA-free, Diethylene Glycol-free, PHO (Partially Hydrogenated Oil)-Free, Persistent Organic Pollutants (POP)-free, Monosodium Glutamate (MSG)-free, Dairy-free, VOC-free, TSE-free, Pareve, Endocrine Disruptor-free, Quaternary Ammonium Salt-Free, Iodide-free, Latex-free, Vegetarian, Non-GMO, Palm Oil-free, Ethylene Glycol-free, Kosher, Dye Free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Organic, Tributyltin (TBT) - Free, APE-free, Pesticide-free, Bisphenol Derivatives-free, CMR Substances-free, Dioxane-free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, PFOS-free, Fungicide-free, BSE-free, Natural Latex Rubber-Free, Vegan, Low Odor

METHOCEL™ K200M Premium HPMC - Specialty 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 SolutionsPOLYOX™ WSR - N80 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, 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 - N80 LEO NF Grade with its off-white color and powder form, exhibits versatile applications. In cosmetics, it functions as both a binder and a thickener, while in industrial additives, it serves similar purposes, offering water solubility for ease of use across various formulations.

METHOCEL™ K15M Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K15M 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, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP, Regulation (EU) No. 1830/2003

METHOCEL™ K15M Modified Cellulose Food Grade - Specialty known for its water solubility, is widely employed in granulation and tablet coating processes. Additionally, it serves as a controlled release agent and film former in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsMETHOCEL™ K100 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:Non-GMO, Palm Oil-free, Phthalates-free, Paraben-free, Nitrosamines-free, Aluminum-free, Mycotoxins-free, Kosher, Preservative-free, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Halal, 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, Dairy-free, VOC-free, Irradiation-free, TSE-free, Glycerin-free, 1,4-Dioxane-free, Pareve, Sugar-free, PFOS-free, Perfluorooctanoic Acid-free, BSE-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Natural Latex Rubber-Free, Dioxin-free, Vegetarian, Tributyl Tin Compounds-Free, Vegan

METHOCEL™ K100 HPMC - Specialty a cellulose ether derivative named Hypromellose, serves as a rheology modifier in industrial applications. Derived from plants, it exhibits water solubility, offering versatility in formulations.

IFF Pharma SolutionsAvicel® PH - 102SCG

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Granules, Suspension
Labeling Claims:Genotoxic-free, Plasticizer-free, Halal, PFOA-free, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Tributyltin (TBT) - Free, Monosodium Glutamate (MSG)-free, Diethylene Glycol-free, Iodide-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Impurities-free, Antibiotics-free, Melamine-free, Fragrance allergen-free, Amine-free, Latex-free, Potassium-free, Fungicide-free, Dioxin-free, Dioxane-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, Bisphenol Derivatives-free, PFAS-Free, Herbicide-free, Non-GMO, PAH-free, Not Tested on Animals, TSE-free, Palm Oil-free, Vegetarian, Pareve, Quaternary Ammonium Salt-Free, Ethylene Oxide-free, Ethylene Glycol-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, CMR Substances-free, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Endocrine Disruptor-free, Glycerin-free
Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), 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, Clean Water Act (CWA) Certified, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Nagoya Compliant, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, FDA 21 CFR 117, 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, Orthodox Union Kosher
Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression

Avicel® PH - 102SCG is a microcrystalline cellulose used in direct compression, dry granulation, and wet granulation manufacturing technologies. It is essential for producing high-quality pharmaceutical tablets with optimal stability and performance.

IFF Pharma SolutionsPOLYOX™ WSR - 205 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 - 205 LEO NF Grade is an off-white powder used as a binder and thickener in cleaning ingredients and pharmaceuticals. It functions in various dosage forms, including tablets, gels, and osmotic pump tablets, utilizing direct compression technology. It offers water solubility.

METHOCEL™ F450 Modified Cellulose Food Grade - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F450 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, PAH-free, Allergen-free, Residual Solvent -Free, Plant-Based, Irradiation-free, Animal Products-free, Monosodium Glutamate (MSG)-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), Hazard Analysis Critical Control Point (HACCP), FDA 21 CFR 101.9, JECFA (FAO/WHO), European Regulation 396/2005/EC, FSSC 22000, Regulation (EU) No. 231/2012, EC No. 1935/2004, ISO 9001, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, 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, FFDCA, 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), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003

METHOCEL™ F450 Modified Cellulose Food Grade - Specialty a modified cellulose with the chemical name Hypromellose, is utilized in various pharmaceutical and nutraceutical applications. Utilizing granulation and tablet coating manufacturing technologies, it serves as a binder, controlled release agent, film former, gelling agent, and immediate release agent, offering water solubility.

IFF Pharma SolutionsAvicel® DG

Chemical Name:Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Tablets
Labeling Claims:Triphenyl Tin Compounds-Free, Genotoxic-free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Zinc-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Impurities-free, Antibiotics-free, Melamine-free, Colorants-free, Amine-free, Latex-free, Dioxin-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Not Tested on Animals, 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, 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. 1169/2011, Regulation (EU) No. 1272/2008, 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, 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, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, FCC Compliant, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher, Orthodox Union Kosher
Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression

Avicel® DG derived from non-animal sources, is a versatile powder used in tablet manufacturing. Its chemical composition includes calcium, hydrogen phosphate, cellulose, and cellulosics. Employing direct compression or wet granulation techniques, it functions as a binder and compression aid in tablet formulations.

IFF Pharma SolutionsAc-Di-Sol® SDW - 802

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, Halal, TSE-free, Vegetarian, Pareve
Certifications & Compliance:Halal Food Council of Europe, 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® 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.

METHOCEL™ F50 Premium LV HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ F50 Premium LV HPMC - Specialty

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
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, Generally Recognized As Safe (GRAS), 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, 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, Sugar-free, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan, Low Odor

METHOCEL™ F50 Premium LV HPMC - Specialty serves as a versatile ingredient in various industries, functioning as a binder, controlled release agent, film former, gelling agent, immediate release agent, mucoadhesive, and solubilizer. Its water solubility makes it suitable for suspensions and various manufacturing processes.

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