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IFF Pharma Solutions
POLYOX™ WSR - 301 LEO NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
POLYOX™ WSR - N80 LEO NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
PRONOVA® UP LVG
Chemical Name:
Sodium Alginate
Dosage Form:
Foams
Labeling Claims:
Kosher, Biocompatible, High Purity, Halal, Biodegradable
Certifications & Compliance:
ISO 14001, National Formulary (NF), Hazard Analysis Critical Control Point (HACCP), European Pharmacopeia (Ph. Eur.), ISO 9000, United States Pharmacopeia (USP), GMP, Directive 2023/2055/EU, EC No.1907/2006
Manufacturing Technology:
Encapsulation
PRONOVA® UP LVG is available in foam form with labeling claims of high purity and biodegradability. It contains sodium alginate, serves as an emulsifier and stabilizer, and is a is a modified and controlled release excipient. The product is supplied in solution form.
IFF Pharma Solutions
Protanal® Ester S 2575
Chemical Name:
Propyleneglycol alginate
CAS Number:
9005-37-2
Labeling Claims:
Colorants-free, Natural Latex Rubber-Free, Copper-free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Gold-Free, Cobalt-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant, EC No.1907/2006
Chemical Inventories:
KECI (Korea), ENCS (Japan), DSL (Canada), IECSC (China), AICS (Australia), NDSL (Canada), PICCS (Phillipines)
Protanal® Ester S 2575 belonging to the alginates chemical family and sourced from non-animal origins, boasts several labeling claims, including being aluminum-free, antibiotic-free, APE-free, bisphenol-A-free, caffeine-free, colorant-free, and dioxin-free.
IFF Pharma Solutions
POLYOX™ WSR - 205 LEO NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
POLYOX™ WSR - N60K LEO NF Grade
Chemical Name:
Polyethylene Oxide, Pyrogenic Silica
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
CELSENTIAL™ E5 Premium LV HPMC
Chemical Name:
Hydroxypropyl Methylcellulose
Functions:
Viscosity Modifier
CAS Number:
9004-65-3
Labeling Claims:
Odor-free, Kosher, CMR Substances-free, Halal, Endocrine Disruptor-free, TSE-free, BSE-free
Certifications & Compliance:
FDA Food Safety Modernization Act (FSMA), Indian Pharmacopeia, IFANCA Halal, Directive 2002/95/EC, FDA 21 CFR 172.874, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), REACH Exempt (Europe), Directive 2011/65/EU (RoHS 2), Directive 2001/83/EC, Directive 1333/2008/EC, GMP, Turkish RoHS Regulation, Directive 2023/2055/EU, Kosher, EC No.1907/2006
CELSENTIAL™ E5 Premium LV HPMC, a cellulose ether known as hypromellose, adeptly modifies viscosity. It's certified BSE-free and CMR substance-free, guaranteeing safety and adherence to strict regulatory standards.
IFF Pharma Solutions
POLYOX™ WSR - N10 NF Grade
Chemical Name:
Polyethylene Oxide, Pyrogenic Silica
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
METHOCEL™ K15M Modified Cellulose Food Grade - Specialty
Chemical Name:
Hydroxypropyl Methylcellulose
Functions:
Controlled Release Agent
Labeling Claims:
Dairy-free, Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Organic, Hypoallergenic, Pareve, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Plant-Based, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), VOC-free, Paraben-free, Dioxin-free, Zero Calorie, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, Low Odor, Kosher, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:
Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, JECFA (FAO/WHO), GMP, FEMA Compliant, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Swiss Ordinance (SR 817.023.21), Directive 1333/2008/EC, Directive 2023/2055/EU, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, FDA 21 CFR 176.180, FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), cGMP, FSSC 22000, FDA 21 CFR 182.1480, Orthodox Union Kosher, EC No. 2023/2006, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, Regulation (EC) No. 1333/2008, EC No.1907/2006
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.
IFF Pharma Solutions
POLYOX™ WSR - 303 LEO NF Grade HV Select
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Vegetarian, Residual Solvent -Free, Halal, Gluten-free, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, TSE-free, Herbicide-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, Fungicide-free, BSE-free, Not Tested on Animals, Pesticide-free, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, ICH Q3C, EC No.1907/2006, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
POLYOX™ WSR - 303 LEO NF Grade HV Select Amerchol composed of ethylene oxide copolymers and polyethylene oxide, serves diverse functions in pharmaceutical formulations. It finds application in abuse-deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. This versatile ingredient acts as a binder, thickener, and controlled release agent, ensuring optimal performance. Available in powder form, it demonstrates water solubility, facilitating easy integration into formulations for enhanced effectiveness.
IFF Pharma Solutions
POLYOX™ WSR - N12K LEO NF Grade
Chemical Name:
Polyethylene Oxide
CAS Number:
25322-68-3
Functions:
Lubricant (Internal), Binder, Flocculant, Film Former, Controlled Release Agent
Dosage Form:
Gels, Tablets, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:
Naturally Derived, Vegetarian, Residual Solvent -Free, Halal, Non-GMO, Allergen-free, Vegan, Dairy-free, Not Listed In California Proposition 65, Heavy Metal-free, TSE-free, Oxidatively Degradable, Kosher, Animal Products-free, Ethylene Glycol-free, BSE-free, Not Tested on Animals, Plant-Based, Diethylene Glycol-free, Chlorine-free, Doping Substances-free, Nitrosamines-free, Zinc-free, No Added Formaldehyde
Certifications & Compliance:
Japan Pharmacopeia (JP), Directive 2002/95/EC, FFDCA, EC No. 2023/2006, Kosher, Japan DMF, ICH Q3C, EC No.1907/2006, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, EC No. 1935/2004, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), US DMF, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), ICH Q3D, EXCiPACT, Clean Water Act (CWA) Certified, Directive 2001/83/EC, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), Directive 2023/2055/EU, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Generally Recognized As Safe (GRAS)
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.
IFF Pharma Solutions
ETHOCEL™ Standard 10 HP Premium Ethylcellulose
Chemical Name:
Ethylcellulose
CAS Number:
9004-57-3
Functions:
Controlled Release Agent, Binder, Granulation Aid, Taste Masker
Labeling Claims:
PFAS-Free, Potassium-free, Aluminum-free, PFOA-free, Dye Free, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Quaternary Ammonium Salt-Free, Vegetarian, Halal, Tributyltin (TBT) - Free, Dioxane-free, FSSC 22000, Paraben-free, PAH-free, PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Phthalates-free, PHO (Partially Hydrogenated Oil)-Free, Sugar-free, Antibiotics-free, 1,4-Dioxane-free, Kosher, Hormones-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Bisphenol Derivatives-free, Organic, Irradiation-free, Non-Mutagenic, Non-Irritant, PVC-free, Iodide-free, VOC-free
Certifications & Compliance:
Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), Kosher, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, EuPIA Listed, FDA 21 CFR 117, Directive 1333/2008/EC, Halal, RoHS Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, FDA 21 CFR 172.868, Regulation (EU) No. 1272/2008, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 73.1001, CFDA Compliant (China), Directive 2012/19/EU, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, FCC Compliant, ISO 9000, USDA Organic, EXCiPACT, EFSA (European Food Safety Authority) Certified, FDA 21 CFR 73.1, Directive 2009/48/EC, British Pharmacopeia (BP), FSC Certified
Manufacturing Technology:
Tablet Coating, Direct Compression, Granulation, Encapsulation
ETHOCEL™ Standard 10 HP Premium Ethylcellulose is ideal for phenolics, modified rosins, alkyds (Long Oil), and fluid bed coating applications. Notable features include excellent adhesion, good green strength, high gloss, good printability, and reduced tack, ensuring superior performance and finish in industrial processes.
IFF Pharma Solutions
PRONOVA® UP LVM
Chemical Name:
Sodium Alginate
Dosage Form:
Foams
Labeling Claims:
Kosher, Biocompatible, High Purity, Halal, Biodegradable
Certifications & Compliance:
ISO 14001, National Formulary (NF), Hazard Analysis Critical Control Point (HACCP), European Pharmacopeia (Ph. Eur.), ISO 9000, United States Pharmacopeia (USP), GMP, Directive 2023/2055/EU, EC No.1907/2006
Manufacturing Technology:
Encapsulation
PRONOVA® UP LVM is available in foam form with labeling claims of high purity and biodegradability. It contains sodium alginate, serves as an emulsifier and stabilizer, and is a is a modified and controlled release excipient. The product is supplied in solution form.
IFF Pharma Solutions
METHOCEL™ K100M Modified Cellulose Food Grade - Specialty
Chemical Name:
Hydroxypropyl Methylcellulose
Functions:
Controlled Release Agent
Labeling Claims:
Dairy-free, Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Organic, Hypoallergenic, Pareve, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Plant-Based, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), VOC-free, Paraben-free, Dioxin-free, Zero Calorie, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, Low Odor, Kosher, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:
Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, JECFA (FAO/WHO), GMP, FEMA Compliant, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, European Regulation 396/2005/EC, WEEE Directive 2012/19/EU, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Swiss Ordinance (SR 817.023.21), Directive 1333/2008/EC, Directive 2023/2055/EU, FDA 21 CFR 176.170, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), Directive 2023/915/EU, FDA 21 CFR 176.180, FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), cGMP, FSSC 22000, FDA 21 CFR 182.1480, Orthodox Union Kosher, EC No. 2023/2006, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, Regulation (EC) No. 1333/2008, EC No.1907/2006
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.
IFF Pharma Solutions
PRONOVA® UP MVG
Chemical Name:
Sodium Alginate
Dosage Form:
Foams
Labeling Claims:
Kosher, Biocompatible, High Purity, Halal, Biodegradable
Certifications & Compliance:
ISO 14001, National Formulary (NF), Hazard Analysis Critical Control Point (HACCP), European Pharmacopeia (Ph. Eur.), ISO 9000, United States Pharmacopeia (USP), GMP, Directive 2023/2055/EU, EC No.1907/2006
Manufacturing Technology:
Encapsulation
PRONOVA® UP MVG is available in foam form with labeling claims of high purity and biodegradability. It contains sodium alginate, serves as an emulsifier and stabilizer, and is a is a modified and controlled release excipient. The product is supplied in solution form.
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