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103 Products found on IFF Pharma Solutions

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METHOCEL™ E4M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ E4M Modified Cellulose Food Grade - Specialty
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Functions:Lubricant (Internal), Surfactant, Emulsifier, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Film Former
  • Labeling Claims:Colorants-free, Natural Latex Rubber-Free, Naturally Derived, Hormones-free, Glycerin-free, Sewage Sludge Free, Plasticizer-free, Organic, Hypoallergenic, Pareve, Residual Solvent -Free, APE-free, Plant-Based, PAH-free, Antibiotics-free, VOC-free, Paraben-free, Zero Calorie, Bisphenol A-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Tributyl Tin Compounds-Free, Low Odor, Kosher, PFAS-Free, Vegan, Dairy-free, Not Listed In California Proposition 65, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Mycotoxins-free, Caffeine Free, Dye Free, Monosodium Glutamate (MSG)-free, Odor-free, PFOS-free, Allergen-free, Irradiation-free, Non-GMO, Dioxin-free, Sugar-free, Aluminum-free, Triphenyl Tin Compounds-Free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Preservative-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 2022/1396, GMP, Halal, Doping-Free, ISO 9001, Regulation (EU) No. 1829/2003, FDA 21 CFR 175.105, Directive 2023/2055/EU, EU Cosmetic Regulation 1223/2009 Compliant, FFDCA, Organic Certified, Directive 2009/48/EC, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 174.5, Generally Recognized As Safe (GRAS), FDA 21 CFR 175.300, EU Packaging Directive (94/62/EC), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, JECFA (FAO/WHO), ISO 14001, National Formulary (NF), FDA 21 CFR 101.9, Indian Pharmacopeia, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, United States Pharmacopeia (USP), FDA Compliant, ISO 50001, Directive 2001/83/EC, Directive 1333/2008/EC, FDA 21 CFR 176.170, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR 172.874, FCC Compliant, British Pharmacopeia (BP), FDA 21 CFR 176.180, cGMP, FDA 21 CFR 182.1480, 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™ E4M Modified Cellulose Food Grade - Specialty is water-soluble and used in granulation and tablet coating manufacturing. It functions as a binder, controlled release agent, film former, gelling agent, immediate release agent, mucoadhesive, and solubilizer in pharmaceuticals and nutraceuticals.
METHOCEL™ F5 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ F5 Premium LV HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Sustained Release Agent, Controlled Release Agent, Binder, Thickener, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Suspension, Tablets
  • Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ F5 Premium LV HPMC is water-soluble and used in suspensions, granulation, and tablet coating. It functions as a binder, controlled release agent, film former, gelling agent, immediate release agent, mucoadhesive, and solubilizer in pharmaceutical and nutraceutical applications.
Ac-Di-Sol® SD - 711 banner
IFF Pharma SolutionsAc-Di-Sol® SD - 711
  • Chemical Name:Croscarmellose Sodium
  • CAS Number:74811-65-7
  • Dosage Form:Orally Disintegrating Tablets (ODTs), Granules, Capsules
  • Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, USP 232 Elemental Impurities Free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR Regulations, FCC Compliant, British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, FSSC 22000, Orthodox Union Kosher, Regulation (EU) No. 1169/2011, IFANCA Halal, China DMF
  • Manufacturing Technology:Wet Granulation
Ac-Di-Sol® SD - 711 a powdered form of croscarmellose sodium, is utilized as a disintegrant and immediate release agent in pharmaceuticals and nutraceuticals. Its versatility is evident in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs), manufactured through wet granulation techniques.
Viscarin® PH - 209NF banner
IFF Pharma SolutionsViscarin® PH - 209NF
  • Chemical Name:Carrageenan
  • CAS Number:9000-07-1
  • Dosage Form:Soft Gels
  • Labeling Claims:Not Listed In California Proposition 65, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Organic, APE-free, Caffeine Free, Dye Free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-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, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Vegan
  • Certifications & Compliance:FDA 21 CFR 177.1520, European Commission Decision 97/534/EC, European Pharmacopeia (Ph. Eur.), FDA 21 CFR 179.26, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FDA 7 CFR 205.605, ABNT NBR 14725, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1830/2003, IFRA Compliant
  • Manufacturing Technology:Encapsulation
Viscarin® PH - 209NF utilizes encapsulation technology and is GMO-free, non-GMO, BSE-free, TSE-free, and palm oil-free. It caters to healthcare and pharma markets, particularly in oral drug delivery and care solutions. It serves as both an emulsifier and stabilizer and aids in formulation and processing in pharmaceutical and nutraceutical applications, including modified and controlled release formulations.
POLYOX™ WSR - 303 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 303 NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Binder, Thickener, Flocculant, Film Former, Viscosity Modifier, Lubricant, 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 - 303 NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.
SeaGel® CAP - 201 banner
IFF Pharma SolutionsSeaGel® CAP - 201
  • Chemical Name:Carrageenan
  • Functions:Encapsulant, Controlled Release Agent
  • Labeling Claims:Organic, Paraben-free, PFOA-free, Phthalates-free, Non-GMO, Not Listed In California Proposition 65, Fungicide-free, Dye Free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Environmentally Friendly, Natural, Plant-Based, Iodide-free, Aluminum-free, PAH-free, TSE-free, Sustainable, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Bisphenol Derivatives-free, Herbicide-free, Palm Oil-free, APE-free, Clean Label, Tributyltin (TBT) - Free, Preservative-free, Kosher, Sugar-free, Hormones-free, Potassium-free, Naturally Derived, PFAS-Free, Quaternary Ammonium Salt-Free, Vegetarian, Nitrosamines-free, Antibiotics-free, Doping Substances-free, Animal Products-free, Plasticizer-free, Dioxane-free, Allergen-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free, Gluten-free
  • Certifications & Compliance:Directive 1333/2008/EC, Regulation (EU) No. 1829/2003, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, FSSC 22000, ISO 9001, cGMP, Regulation (EU) No. 1272/2008, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Directive 396/2005/EC, FDA 21 CFR 177.1520, Clean Water Act (CWA) Certified, Nagoya Compliant, Orthodox Union Kosher, FDA 21 CFR 179.26
  • Dosage Form:Capsules
SeaGel® CAP - 201 identified as carrageenan, offers versatility and quality in capsule applications. With its natural and non-animal plant origins, it ensures ethical sourcing. Featuring easy-to-use powder form, it boasts film-forming properties, heat, and thermal stability. Additionally, it functions as an encapsulant and controlled release agent, providing enhanced performance in encapsulation processes.
Accelerate® DS - 812 banner
IFF Pharma SolutionsAccelerate® DS - 812
  • Chemical Name:Croscarmellose Sodium, Cellulose Gum
  • Dosage Form:Orally Disintegrating Tablets (ODTs), Granules, Soft Chews, Tablets, Capsules
  • Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Melamine-free, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-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, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
  • Certifications & Compliance:Doping-Free, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FDA 21 CFR Regulations, Nagoya Compliant, FSSC 22000, Orthodox Union Kosher, IFANCA Halal
  • Manufacturing Technology:Wet Granulation
Accelerate® DS - 812 contains cellulose gum and is available in capsule, granule, and orally disintegrating tablet forms. Utilizing wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical applications.
Endurance® VE - 090 banner
IFF Pharma SolutionsEndurance® VE - 090
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Tablets
  • Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Solvent-free, APE-free, Caffeine Free, Dye Free, Mercury-Free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Odor-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-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, Zinc-free, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free
  • Certifications & Compliance:Kosher, Halal, Doping-Free, ISO 14001, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Food Safety Modernization Act (FSMA), ISO 22000, Halal, Central Islamic Council of Thailand, Generally Recognized As Safe (GRAS), FCC Compliant, ISO 45001, cGMP, FSSC 22000, Orthodox Union Kosher, IFANCA Halal
  • Manufacturing Technology:Direct Compression, Wet Granulation
Endurance® VE - 090 is used in dietary supplements, functioning as a binder. It comes with labeling claims of being aluminum-free, antibiotic-free, APE-free, and bisphenol-A-free. Additionally, it serves as a binder in pharmaceuticals and nutraceuticals.
POLYOX™ WSR - N750 LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N750 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 - N750 LEO 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.
ETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty
  • Chemical Family:Cellulose Ethers, Cellulose & Cellulosics
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Pigment Type:Metallic Effect
  • Dosage Form:Tablets
  • Labeling Claims:FSSC 22000, Not Listed In California Proposition 65, Sugar-free, Iodide-free, 1,4-Dioxane-free, Nitrosamines-free, Gluten-free, Quaternary Ammonium Salt-Free, Plasticizer-free, Halal, PFOS-free, Bisphenol Derivatives-free, Caffeine Free, Irradiation-free, Odor-free, VOC-free, PFAS-Free, Kosher, Tributyltin (TBT) - Free, PAH-free, Natural Latex Rubber-Free, Organic, Allergen-free, Dioxane-free, Antibiotics-free, Hormones-free, Dairy-free, Zero Calorie, Monosodium Glutamate (MSG)-free, Phthalates-free, Paraben-free, Non-Mutagenic, Non-Irritant, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, Aluminum-free, Sewage Sludge Free, Potassium-free, PFOA-free, PVC-free, Pesticide-free
  • Color (Properties):White
  • Certifications & Compliance:Chinese Pharmacopeia (ChP), Clean Water Act (CWA) Certified, ICH Q3C, EFSA (European Food Safety Authority) Certified, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, Kosher, ISO 9001, Organic Certified, Regulation (EU) No. 10/2011 (PIM), GMP, Directive 1333/2008/EC, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 117, FSSC 22000, United States Pharmacopeia (USP), FDA Compliant, EuPIA Listed, Regulation (EU) No. 231/2012, USDA Organic, Regulation (EC) No. 1333/2008, FSC Certified, JECFA (FAO/WHO), cGMP, FDA 21 CFR 172.868, RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP), FDA Food Safety Modernization Act (FSMA), EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Directive 2012/19/EU, Regulation (EU) No. 1272/2008, Directive 2009/48/EC, Halal, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, Japan Pharmacopeia (JP), FDA 21 CFR 101.9
  • Manufacturing Technology:Tablet Coating, Direct Compression, Encapsulation, Granulation
ETHOCEL™ Standard 45 Industrial Ethylcellulose - Specialty is optimized for spray, phenolics, and modified rosins applications. It features good printability, reduced tack, and scuff resistance, ensuring high-quality finishes. Serving as a stabilizer and thickener, it is available in both powder and granule forms, presenting a white color for versatility in industrial processes.

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