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47 Products found on IFF Pharma Solutions

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POLYOX™ WSR - 301 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 301 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 301 LEO NF Grade characterized by its off-white color, serves as a binder and thickener in cosmetic formulations. It is available in powder form and exhibits water solubility. Its versatility extends to various dosage forms including abuse deterrent tablets & capsules, gels, and osmotic pump tablets.
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METHOCEL™ K15M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ K15M Modified Cellulose Food Grade - Specialty
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Functions:Controlled Release Agent
  • Labeling Claims:Endocrine Disruptor-free, Glycerin-free, Perfluorooctanoic Acid-free, Hypoallergenic, Triphenyl Tin Compounds-Free, Plasticizer-free, Dairy-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Plant-Based, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Sewage Sludge Free, PFOS-free, Nitrosamines-free, Hormones-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Pesticide-free, Kosher, Antibiotics-free, Naturally Derived, Colorants-free, Dioxin-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Low Odor, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Bisphenol A-free, Generally Recognized As Safe (GRAS), Zero Calorie, APE-free, BSE-free, Irradiation-free, Organic, Sugar-free, PVC-free, Dye Free, CMR Substances-free, VOC-free, Mycotoxins-free
  • Certifications & Compliance:FSSC 22000, cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, FDA 21 CFR 176.180, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), FDA 21 CFR 175.105, USDA Organic, Swiss Ordinance (SR 817.023.21), ICH Q3C, FDA 21 CFR 101.9, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, FDA 21 CFR 172.874, FDA 21 CFR 182.1480, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, Regulation (EU) No. 1829/2003, GMP, FEMA Compliant, Halal, Doping-Free, ISO 14001, National Formulary (NF), Regulation (EC) No. 1333/2008, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, Regulation (EU) No. 1830/2003, Directive 2023/2055/EU, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1935/2004, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FDA 21 CFR 174.5, FDA 21 CFR 175.300, Organic Certified, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, Orthodox Union Kosher, EU Packaging Directive (94/62/EC)
  • Dosage Form:Tablets
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.
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POLYOX™ WSR - N80 LEO NF Grade banner
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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, 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.
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POLYOX™ WSR - 205 LEO NF Grade banner
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, British Pharmacopeia (BP), Directive 2023/2055/EU, 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.
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Protanal® PH - 6610 banner
IFF Pharma SolutionsProtanal® PH - 6610
  • Chemical Name:Sodium Alginate
  • Ingredient Name:Sodium Alginate
  • CAS Number:9005-38-3
  • Labeling Claims:Antibiotics-free, Pareve, Gluten-free, Copper-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Steroids Free, Cobalt-free, Bactericide-free, Propylene Glycol-free, Artificial Flavor-Free, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Perfluorocarbon (PFC)-free, Fungicide-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), Solvent-free, Allergen-free, PAH-free, Residual Solvent -Free, Irradiation-free, Animal Products-free, Melamine-free, Latex-free, Monosodium Glutamate (MSG)-free, Radioactive-free, Phthalates-free, Palm Oil-free, CMR Substances-free, Barium-free, No Artificial Sweeteners, Mycotoxins-free, Dioxin-free, NPE-free, PHO (Partially Hydrogenated Oil)-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Herbicide-free, Cadmium-free, Preservative-free, Quaternary Ammonium Salt-Free, APE-free, PFOS-free, PFOA-free, Mercury-Free, Gold-Free, BSE-free, Impurities-free, Paraben-free, Tin-free, Halal, Tributyltin (TBT) - Free, Non-GMO, GMO-free, Nanomaterials-free, Plasticizer-free, Potassium-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, Doping-Free, European Pharmacopeia (Ph. Eur.), IFRA Compliant, FDA 21 CFR 117, EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), ISO 14001, cGMP, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, Kosher, FFDCA, National Formulary (NF), Halal Food Council of Europe, EC No. 2023/2006, FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, ISO 9000, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, British Pharmacopeia (BP), GMP
Protanal® PH - 6610 is a versatile solution for various industries. This product is sewage-sludge-free, ensuring purity and safety. In pharmaceuticals and nutraceuticals, it acts as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid, offering multifaceted benefits.
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POLYOX™ WSR - N12K LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N12K LEO NF Grade is an off-white powder with water-soluble properties. It's used as a binder and thickener in cleaning products and pharmaceuticals. Its applications include gels, osmotic pump tablets, and regular tablets, and it's manufactured using direct compression technology. Additionally, it serves as a controlled release agent.
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POLYOX™ WSR - N10 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N10 NF Grade
  • Chemical Name:Polyethylene Oxide, Pyrogenic Silica
  • 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N10 NF Grade is an off-white powder with water-soluble properties. It's used as a binder and thickener in cleaning products and pharmaceuticals. Its applications include gels, osmotic pump tablets, and regular tablets, and it's manufactured using direct compression technology. Additionally, it serves as a controlled release agent.
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POLYOX™ WSR - N60K LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N60K LEO NF Grade
  • Chemical Name:Polyethylene Oxide, Pyrogenic Silica
  • 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N60K LEO 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.
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METHOCEL™ F450 Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ F450 Modified Cellulose Food Grade - Specialty
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Functions:Lubricant (Internal), Film Former, Rheology Modifier, Surfactant, Emulsifier, Binder, Plasticizer, Controlled Release Agent
  • Labeling Claims:Monosodium Glutamate (MSG)-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Pesticide-free, Antibiotics-free, Naturally Derived, Colorants-free, Dioxin-free, Animal Products-free, Low Odor, Non-GMO, Tributyl Tin Compounds-Free, Pareve, Bisphenol A-free, Organic, Sugar-free, PVC-free, Dye Free, CMR Substances-free, Endocrine Disruptor-free, Glycerin-free, Perfluorooctanoic Acid-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Dairy-free, Halal, Paraben-free, Allergen-free, Aflatoxin-free, Sewage Sludge Free, PFOS-free, Vegan, Caffeine Free, Kosher, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, PAH-free, TSE-free, Palm Oil-free, Vegetarian, Zero Calorie, APE-free, BSE-free, Irradiation-free, VOC-free, Mycotoxins-free, Hypoallergenic, Aluminum-free, Preservative-free, Plant-Based
  • Certifications & Compliance:FDA 21 CFR 176.180, EC No. 1935/2004, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), USDA Organic, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, EC No. 2023/2006, Kosher, GMP, Halal, Doping-Free, Regulation (EC) No. 1333/2008, ISO 9001, EU Directive 2002/72/EC, Directive 2023/2055/EU, Regulation (EU) No. 10/2011 (PIM), EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 174.5, FDA 21 CFR 175.300, Organic Certified, Directive 2009/48/EC, Orthodox Union Kosher, EU Packaging Directive (94/62/EC), FFDCA, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008, FDA 21 CFR 175.105, ICH Q3C, FDA 21 CFR 101.9, FDA 21 CFR 172.874, FDA 21 CFR 182.1480, JECFA (FAO/WHO), Regulation (EU) No. 1829/2003, ISO 14001, National Formulary (NF), Indian Pharmacopeia, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, United States Pharmacopeia (USP), FDA Compliant, REACH Exempt (Europe), ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, FDA 21 CFR 176.170, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), FCC Compliant, British Pharmacopeia (BP), cGMP, Regulation (EU) No. 1169/2011
  • Dosage Form:Tablets
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.
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METHOCEL™ K100M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ K100M Modified Cellulose Food Grade - Specialty
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Functions:Controlled Release Agent
  • Labeling Claims:Endocrine Disruptor-free, Glycerin-free, Perfluorooctanoic Acid-free, Hypoallergenic, Triphenyl Tin Compounds-Free, Plasticizer-free, Dairy-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Plant-Based, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Sewage Sludge Free, PFOS-free, Nitrosamines-free, Hormones-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Pesticide-free, Kosher, Antibiotics-free, Naturally Derived, Colorants-free, Dioxin-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Low Odor, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Bisphenol A-free, Generally Recognized As Safe (GRAS), Zero Calorie, APE-free, BSE-free, Irradiation-free, Organic, Sugar-free, PVC-free, Dye Free, CMR Substances-free, VOC-free, Mycotoxins-free
  • Certifications & Compliance:FSSC 22000, cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, FDA 21 CFR 176.180, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), FDA 21 CFR 175.105, USDA Organic, Swiss Ordinance (SR 817.023.21), ICH Q3C, FDA 21 CFR 101.9, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, FDA 21 CFR 172.874, FDA 21 CFR 182.1480, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, Regulation (EU) No. 1829/2003, GMP, FEMA Compliant, Halal, Doping-Free, ISO 14001, National Formulary (NF), Regulation (EC) No. 1333/2008, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, Regulation (EU) No. 1830/2003, Directive 2023/2055/EU, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1935/2004, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FDA 21 CFR 174.5, FDA 21 CFR 175.300, Organic Certified, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, Orthodox Union Kosher, EU Packaging Directive (94/62/EC)
  • Dosage Form:Tablets
METHOCEL™ K100M Modified Cellulose Food Grade - Specialty known chemically as hypromellose, demonstrates water solubility and finds applications across various pharmaceutical and nutraceutical functions. It acts as a gelling agent, immediate release agent, mucoadhesive, solubilizer, sustained release agent, and viscosity modifier. Its versatility makes it suitable for use in granulation, tablet coating, and other formulation processes in the food industry.
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ETHOCEL™ Standard 10 Premium Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 10 Premium Ethylcellulose - Specialty
  • INCI Name:Ethylcellulose
  • Ingredient Name:Ethyl Cellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • Chemical Name:Ethylcellulose
  • Ingredient Origin:Plant Origin
  • CAS Number:9004-57-3
  • Labeling Claims:PFOS-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, Vegan, GMO-free, Zero Calorie, Plant-Based, Mycotoxins-free, Pesticide-free, Hormones-free, APE-free, Sugar-free, Perfluorooctanoic Acid-free, Monosodium Glutamate (MSG)-free, Plasticizer-free, Animal Products-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Paraben-free, Phthalates-free, Formaldehyde-free, 1,4-Dioxane-free, PAH-free, Halal, PVC-free, Aluminum-free, PFAS-Free, Antibiotics-free, Aflatoxin-free, Non-Irritant, Non-Mutagenic, Caffeine Free, Organic, Irradiation-free, VOC-free, Endocrine Disruptor-free, Vegetarian, Tributyl Tin Compounds-Free, Allergen-free, Solvent-free, Natural Latex Rubber-Free, Nitrosamines-free, TSE-free, Non-GMO, Naturally Derived, Kosher, CMR Substances-free, Colorants-free, Sewage Sludge Free, Dye Free, Dioxin-free, Preservative-free, Palm Oil-free, BSE-free
  • Certifications & Compliance:FDA 21 CFR 163, EXCiPACT, Regulation (EU) No. 10/2011 (PIM), Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant, Canadian Environmental Protection Act (CEPA), Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, US FDA Compliance Policy Guide Section 560.750, Regulation (EU) No. 1829/2003, FDA 21 CFR 573.420, Orthodox Union Kosher, Clean Air Act (CAA) Certified, RoHS Compliant, Japan Chemical Substances Control Law (CSCL), European Regulation 396/2005/EC, RoHS 2 Compliant, EC No. 1935/2004, Regulation (EU) No. 1830/2003, Directive 2001/18/EC, cGMP, Japan Pharmacopeia (JP), FCC Compliant, Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), JECFA (FAO/WHO), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, WEEE Directive 2012/19/EU, Organic Certified, Regulation (EU) No. 1272/2008, Majelis Ulama Indonesia Halal, Halal, FDA Compliant, Turkish RoHS Regulation, CFDA Compliant (China), Doping-Free, USDA Organic, FDA 21 CFR 73.1001, Kosher, Directive 2009/48/EC, Regulation (EU) No. 1169/2011, GMP, ICH Q3C, EuPIA Listed, ICH Q3D, FSSC 22000, Regulation (EC) No. 1333/2008, ISO 9000, Belgian Law And Codex Alimentarius Standards, Swiss Ordinance (SR 817.023.21), FDA 21 CFR 172.868, Hazard Analysis Critical Control Point (HACCP), Generally Recognized As Safe (GRAS), FDA 21 CFR 181.24, National Formulary (NF), ISO 9001, British Pharmacopeia (BP), EU Directive 2002/72/EC
ETHOCEL™ Standard 10 Premium Ethylcellulose - Specialty characterized by its white color, serves as a stabilizer and thickener in cosmetic ingredients. Utilizing encapsulation, granulation, hot melt extrusion, and tablet coating technologies, it is available in a powdered physical form.
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POLYOX™ WSR - N750 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N750 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, Kosher, ICH Q3C, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, Generally Recognized As Safe (GRAS), EXCiPACT, Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N750 NF Grade is available in various dosage forms including gels, osmotic pump tablets, and traditional tablets. Utilizing direct compression manufacturing technology, it serves applications in both oral and topical drug delivery within the healthcare and pharmaceutical markets. With its properties as a binder and thickener, this white, water-soluble powder aids in formulation processes.
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Protanal® PH - 6160 banner
IFF Pharma SolutionsProtanal® PH - 6160
  • Chemical Name:Sodium Alginate
  • Ingredient Name:Sodium Alginate
  • CAS Number:9005-38-3
  • Labeling Claims:Antibiotics-free, Pareve, Gluten-free, Copper-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Steroids Free, Cobalt-free, Bactericide-free, Propylene Glycol-free, Artificial Flavor-Free, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Perfluorocarbon (PFC)-free, Fungicide-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), Solvent-free, Allergen-free, PAH-free, Residual Solvent -Free, Irradiation-free, Animal Products-free, Melamine-free, Latex-free, Monosodium Glutamate (MSG)-free, Radioactive-free, Odor-free, Phthalates-free, Palm Oil-free, CMR Substances-free, Barium-free, No Artificial Sweeteners, Mycotoxins-free, Dioxin-free, NPE-free, PHO (Partially Hydrogenated Oil)-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Herbicide-free, Cadmium-free, Preservative-free, Quaternary Ammonium Salt-Free, APE-free, PFOS-free, PFOA-free, Mercury-Free, Gold-Free, BSE-free, Impurities-free, Paraben-free, Tin-free, Halal, Tributyltin (TBT) - Free, Non-GMO, GMO-free, Nanomaterials-free, Plasticizer-free, Potassium-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, Doping-Free, European Pharmacopeia (Ph. Eur.), IFRA Compliant, FDA 21 CFR 117, EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), ISO 14001, cGMP, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, Kosher, FFDCA, National Formulary (NF), EC No. 2023/2006, FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, ISO 9000, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, British Pharmacopeia (BP), GMP
  • Chemical Inventories:NDSL (Canada), IECSC (China), PICCS (Phillipines), DSL (Canada), ECL (Korea), AICS (Australia), ENCS (Japan)
Protanal® PH - 6160 is a versatile ingredient suitable for various applications. This powder is swage-sludge-free, ensuring purity and safety. In pharmaceuticals and nutraceuticals, it serves as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid, offering multifunctional benefits.
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Protanal® Ester K3B426 banner
IFF Pharma SolutionsProtanal® Ester K3B426
  • Chemical Name:Propyleneglycol alginate
  • CAS Number:9005-37-2
  • Labeling Claims:Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, Aflatoxin-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, Melamine-free, Barium-free, Cadmium-free, Colorants-free, Latex-free, Dioxin-free, Cobalt-free, Animal Products-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, Propylene Glycol-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, BSE-free, Sugar-free, PVC-free, Dye Free, Nanomaterials-free, Mycotoxins-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, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, Regulation (EU) No. 1829/2003, GMP, 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, Regulation (EU) No. 1830/2003, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1935/2004, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), EU Packaging Directive (94/62/EC), FSSC 22000, Hazard Analysis Critical Control Point (HACCP)
Protanal® Ester K3B426 ensures peace of mind with its labeling claims of being free from bisphenol A, caffeine, colorants, and dioxin. This versatile powder serves multiple functions in pharmaceuticals, belonging to both excipients and active pharmaceutical ingredients (APIs) categories.
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Protanal® PH - 1322 banner
IFF Pharma SolutionsProtanal® PH - 1322
  • Chemical Name:Sodium Alginate
  • Ingredient Name:Sodium Alginate
  • CAS Number:9005-38-3
  • Labeling Claims:Antibiotics-free, Pareve, Gluten-free, Copper-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, Vegetarian, Kosher, Steroids Free, Cobalt-free, Bactericide-free, Propylene Glycol-free, Artificial Flavor-Free, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Perfluorocarbon (PFC)-free, Fungicide-free, Pesticide-free, Sugar-free, Generally Recognized As Safe (GRAS), Solvent-free, Allergen-free, PAH-free, Residual Solvent -Free, Irradiation-free, Animal Products-free, Melamine-free, Latex-free, Monosodium Glutamate (MSG)-free, Radioactive-free, Phthalates-free, Palm Oil-free, CMR Substances-free, Barium-free, No Artificial Sweeteners, Mycotoxins-free, Dioxin-free, NPE-free, PHO (Partially Hydrogenated Oil)-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Herbicide-free, Cadmium-free, Preservative-free, Quaternary Ammonium Salt-Free, APE-free, PFOS-free, PFOA-free, Mercury-Free, Gold-Free, BSE-free, Impurities-free, Paraben-free, Tin-free, Halal, Tributyltin (TBT) - Free, Non-GMO, GMO-free, Nanomaterials-free, Plasticizer-free, Potassium-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, Doping-Free, European Pharmacopeia (Ph. Eur.), IFRA Compliant, FDA 21 CFR 117, EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), ISO 14001, cGMP, FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, Kosher, FFDCA, National Formulary (NF), Halal Food Council of Europe, EC No. 2023/2006, FCC Compliant, Generally Recognized As Safe (GRAS), EXCiPACT, ISO 9000, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, British Pharmacopeia (BP), GMP
Protanal® PH - 1322 is a versatile powder offering various functions for pharmaceuticals and nutraceuticals. It serves as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid. It's also sewage-sludge-free, ensuring purity.
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