Drug Delivery & Care Solutions

129 Products found in Drug Delivery & Care Solutions

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IFF Pharma SolutionsMETHOCEL™ K4M Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Labeling Claims:Sugar-free, Low Odor, Palm Oil-free, Dioxin-free, Pesticide-free, APE-free, Kosher, Endocrine Disruptor-free, Vegan, PAH-free, Natural Latex Rubber-Free, Antibiotics-free, Dye Free, PFAS-Free, Colorants-free, CMR Substances-free, USP 232 Elemental Impurities Free, TSE-free, Paraben-free, Triphenyl Tin Compounds-Free, BSE-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Halal, Bisphenol A-free, PVC-free, Vegetarian, Naturally Derived, Hormones-free, Zero Calorie, Plasticizer-free, Hypoallergenic, Perfluorooctanoic Acid-free, Mycotoxins-free, Aflatoxin-free, Aluminum-free, Phthalates-free, PFOS-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, British Pharmacopeia (BP), JECFA (FAO/WHO), GMP, FDA 21 CFR 172.874, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Halal, Kosher, EU Packaging Directive (94/62/EC), Swiss Ordinance (SR 817.023.21), CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), WEEE Directive 2012/19/EU, FEMA Compliant, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), National Formulary (NF), European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, EXCiPACT, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, ISO 14001
Manufacturing Technology:Granulation

METHOCEL™ K4M Premium HPMC utilized in ceramics and pharmaceuticals, serves as a binder, film former, gelling agent, mucoadhesive, solubilizer, and suspension aid. It aids in granulation and exhibits water solubility.

IFF Pharma SolutionsManugel® DMB

Chemical Name:Sodium Alginate
Labeling Claims:Palm Oil-free, Barium-free, GMO-free, Dioxin-free, Copper-free, Pesticide-free, APE-free, Gold-Free, Allergen-free, Kosher, Endocrine Disruptor-free, Vegan, PAH-free, Natural Latex Rubber-Free, Mercury-Free, Antibiotics-free, Dye Free, PFAS-Free, Colorants-free, Gluten-free, TSE-free, Paraben-free, Nitrosamines-free, Triphenyl Tin Compounds-Free, BSE-free, Residual Solvent -Free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Melamine-free, Irradiation-free, Halal, Bisphenol A-free, PVC-free, Vegetarian, Cadmium-free, Latex-free, Hormones-free, Heavy Metal-free, Plasticizer-free, Perfluorooctanoic Acid-free, Non-GMO, Formaldehyde-free, Aflatoxin-free, Aluminum-free, Phthalates-free, PFOS-free, Tributyl Tin Compounds-Free, Cobalt-free, Sugar-free
Certifications & Compliance:EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Kosher, Doping-Free, European Regulation 396/2005/EC, National Formulary (NF), FDA Food Safety Modernization Act (FSMA), IFRA Compliant, Regulation (EU) No. 231/2012, Generally Recognized As Safe (GRAS)

Manugel® DMB is free from copper, cobalt, barium, and gold. It serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsSeaGel® CAP - 101

Chemical Name:Carrageenan
Functions:Encapsulant, Controlled Release Agent
Labeling Claims:Environmentally Friendly, Pesticide-free, Nitrosamines-free, Palm Oil-free, Kosher, Paraben-free, GMO-free, Sugar-free, Naturally Derived, Perfluorooctanoic Acid-free, Tributyl Tin Compounds-Free, Phthalates-free, Sustainable, PFOS-free, PAH-free, APE-free, Non-GMO, Plasticizer-free, Halal, Vegetarian, Generally Recognized As Safe (GRAS), Aluminum-free, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Caffeine Free, Antibiotics-free, Bisphenol A-free, Dye Free, TSE-free, Hormones-free, Natural, Natural Latex Rubber-Free, PVC-free, Vegan, Triphenyl Tin Compounds-Free, Endocrine Disruptor-free, Preservative-free, PFAS-Free, Glycerin-free, Dioxin-free, Monosodium Glutamate (MSG)-free, Colorants-free
Certifications & Compliance:IFRA Compliant, Regulation (EU) No. 1272/2008, Doping-Free, Regulation (EU) No. 1169/2011, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EU Cosmetic Regulation 1223/2009 Compliant, Halal, FDA Food Safety Modernization Act (FSMA)
Dosage Form:Capsules

SeaGel® CAP - 101 ideal for capsules, utilizes encapsulation technology. It meets labeling claims like non-GMO, BSE-free, TSE-free, palm oil-free, glycerin-free, and endocrine disruptor-free, ensuring suitability for vegetarians. Its applications span food, nutrition, healthcare, and pharmaceuticals, serving in nutraceuticals, supplements, and oral drug delivery.

IFF Pharma SolutionsAccelerate® DS - 813

Chemical Name:Cellulose Gum
Functions:Disintegrant
Manufacturing Technology:Wet Granulation
Labeling Claims:Dye Free, Antibiotics-free, Monosodium Glutamate (MSG)-free, Paraben-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Not Listed In California Proposition 65, Generally Recognized As Safe (GRAS), PAH-free, TSE-free, GMO-free, Pesticide-free, Dioxin-free, Perfluorooctanoic Acid-free, Colorants-free, Glycerin-free, BSE-free, Hormones-free, Natural Latex Rubber-Free, Endocrine Disruptor-free, PFAS-Free, Ethylene Oxide-free, PFOS-free, Tributyl Tin Compounds-Free, APE-free, Aluminum-free, Nanomaterials-free, Melamine-free, Preservative-free, Sugar-free, Plasticizer-free, Palm Oil-free, PVC-free, Triphenyl Tin Compounds-Free, Caffeine Free, Phthalates-free, Bisphenol A-free, Non-GMO, Vegetarian
Certifications & Compliance:ICH Q3C, Nagoya Compliant, Regulation (EU) No. 231/2012, European Pharmacopeia (Ph. Eur.), European Regulation 396/2005/EC, FDA 21 CFR Regulations, FDA Food Safety Modernization Act (FSMA), United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, cGMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Doping-Free

Accelerate® DS - 813 is available in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs). Manufactured using wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical formulations. It is supplied in powder form for ease of processing and formulation.

IFF Pharma SolutionsMETHOCEL™ A4M Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Labeling Claims:Sugar-free, Low Odor, Palm Oil-free, Dioxin-free, Pesticide-free, APE-free, Allergen-free, Kosher, Endocrine Disruptor-free, Odor-free, Vegan, PAH-free, Natural Latex Rubber-Free, Antibiotics-free, Dye Free, PFAS-Free, Colorants-free, Gluten-free, USP 232 Elemental Impurities Free, TSE-free, Paraben-free, Nitrosamines-free, Triphenyl Tin Compounds-Free, BSE-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Melamine-free, Halal, Bisphenol A-free, PVC-free, Vegetarian, Naturally Derived, Hormones-free, Zero Calorie, Plasticizer-free, Hypoallergenic, Perfluorooctanoic Acid-free, Mycotoxins-free, Aflatoxin-free, Not Listed In California Proposition 65, Aluminum-free, Phthalates-free, PFOS-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, British Pharmacopeia (BP), GMP, FDA 21 CFR 172.874, Regulation (EU) No. 1272/2008, Halal, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), National Formulary (NF), European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, EXCiPACT, Japan Pharmacopeia (JP), ISO 14001
Manufacturing Technology:Granulation, Wet Granulation

METHOCEL™ A4M Premium Methylcellulose a water-soluble additive, is utilized in granulation and wet granulation manufacturing. It functions as a binder in ceramics and pharmaceuticals, serving as a binder, film former, and gelling agent in various applications.

IFF Pharma SolutionsViscarin® PH - 109NF

Chemical Name:Carrageenan
CAS Number:9000-07-1
Dosage Form:Soft Gels
Labeling Claims:Non-GMO, Aluminum-free, Phthalates-free, PFOS-free, Tributyl Tin Compounds-Free, TSE-free, Paraben-free, Nitrosamines-free, Triphenyl Tin Compounds-Free, Sugar-free, BSE-free, Palm Oil-free, GMO-free, Dioxin-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Pesticide-free, APE-free, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Endocrine Disruptor-free, Bisphenol A-free, PVC-free, Vegetarian, Vegan, PAH-free, Natural Latex Rubber-Free, Hormones-free, Antibiotics-free, Dye Free, PFAS-Free, Plasticizer-free, Colorants-free, Perfluorooctanoic Acid-free
Certifications & Compliance:European Regulation 396/2005/EC, National Formulary (NF), European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1169/2011, IFRA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Regulation (EU) No. 231/2012, ABNT NBR 14725, Doping-Free
Manufacturing Technology:Encapsulation

Viscarin® PH - 109NF employing encapsulation technology, offers BSE-free, TSE-free, palm oil-free, and glycerin-free formulations. It serves as a controlled release agent, encapsulant, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsEndurance® VE - 102

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

Endurance® VE - 102 comprising microcrystalline cellulose, finds applications in dietary supplements. It functions as a binder in food and nutrition, as well as in pharmaceuticals and nutraceuticals, presenting as a powder.

IFF Pharma SolutionsMETHOCEL™ K100 Premium LVCR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Suspension
Labeling Claims:Sugar-free, Low Odor, Palm Oil-free, Dioxin-free, Pesticide-free, APE-free, Kosher, Endocrine Disruptor-free, Odor-free, Vegan, PAH-free, Natural Latex Rubber-Free, Antibiotics-free, Dye Free, PFAS-Free, Colorants-free, CMR Substances-free, USP 232 Elemental Impurities Free, TSE-free, Paraben-free, Triphenyl Tin Compounds-Free, BSE-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Halal, Bisphenol A-free, PVC-free, Vegetarian, Naturally Derived, Hormones-free, Zero Calorie, Plasticizer-free, Hypoallergenic, Perfluorooctanoic Acid-free, Mycotoxins-free, Aflatoxin-free, Aluminum-free, Phthalates-free, PFOS-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, British Pharmacopeia (BP), JECFA (FAO/WHO), GMP, FDA 21 CFR 172.874, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Halal, Kosher, EU Packaging Directive (94/62/EC), Swiss Ordinance (SR 817.023.21), CFDA Compliant (China), ABNT NBR 14725, Doping-Free, United States Pharmacopeia (USP), WEEE Directive 2012/19/EU, FEMA Compliant, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), National Formulary (NF), European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, Regulation (EU) No. 2022/1396, ICH Q3C, EXCiPACT, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, ISO 14001
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K100 Premium LVCR HPMC belonging to the cellulose ether chemical family, is manufactured using granulation technology. In pharmaceuticals and nutraceuticals, it serves as a controlled release agent, film former, gelling agent, immediate release agent, and mucoadhesive, offering water solubility for diverse applications.

IFF Pharma SolutionsPOLYOX™ WSR - N60K SFP NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Dosage Form:Tablets, Gels, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:Residual Solvent -Free, Ethylene Glycol-free, Not Tested on Animals, Allergen-free, Halal, Kosher, No Added Formaldehyde, Vegetarian, Diethylene Glycol-free, Vegan, Chlorine-free, Naturally Derived, Heavy Metal-free, Not Listed In California Proposition 65, Plant-Based, Nitrosamines-free
Certifications & Compliance:Japan DMF, British Pharmacopeia (BP), Belgian Law And Codex Alimentarius Standards, Chinese Pharmacopeia (ChP), GMP, Halal, Kosher, CFDA Compliant (China), ICH Q3C, United States Pharmacopeia (USP), EXCiPACT, Clean Water Act (CWA) Certified, Japan Pharmacopeia (JP), US DMF, National Formulary (NF), ICH Q3D, European Pharmacopeia (Ph. Eur.)
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 - 205 FP NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Dosage Form:Tablets, Gels, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:Residual Solvent -Free, Ethylene Glycol-free, Not Tested on Animals, Pesticide-free, Fungicide-free, Allergen-free, Vegetarian, Diethylene Glycol-free, Vegan, Chlorine-free, Dairy-free, Gluten-free, Not Listed In California Proposition 65, Nitrosamines-free, Herbicide-free
Certifications & Compliance:British Pharmacopeia (BP), Belgian Law And Codex Alimentarius Standards, Chinese Pharmacopeia (ChP), GMP, FDA Compliant, ICH Q3C, United States Pharmacopeia (USP), EXCiPACT, Clean Water Act (CWA) Certified, Japan Pharmacopeia (JP), National Formulary (NF), European Pharmacopeia (Ph. Eur.)

POLYOX™ WSR - 205 FP NF Grade comprising ethylene oxide copolymers and polyethylene oxide (PEG-14M), serves multiple functions across various pharmaceutical applications. Its versatility extends to deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. Functioning as a binder and thickener, it ensures optimal formulation performance. Available in powder form, it exhibits water solubility, facilitating ease of use in pharmaceutical formulations.

IFF Pharma SolutionsPOLYOX™ WSR - 303 NF TG LEO

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Dosage Form:Tablets, Gels, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:Residual Solvent -Free, Ethylene Glycol-free, Not Tested on Animals, Allergen-free, Halal, Kosher, No Added Formaldehyde, Vegetarian, Diethylene Glycol-free, Vegan, Chlorine-free, Naturally Derived, Heavy Metal-free, Not Listed In California Proposition 65, Plant-Based, Nitrosamines-free
Certifications & Compliance:Japan DMF, British Pharmacopeia (BP), Belgian Law And Codex Alimentarius Standards, Chinese Pharmacopeia (ChP), GMP, Halal, Kosher, CFDA Compliant (China), ICH Q3C, United States Pharmacopeia (USP), EXCiPACT, Clean Water Act (CWA) Certified, Japan Pharmacopeia (JP), US DMF, National Formulary (NF), ICH Q3D, European Pharmacopeia (Ph. Eur.)
Manufacturing Technology:Direct Compression

POLYOX™ WSR - 303 NF TG LEO featuring an off-white color and a powder physical form, serves as a binder and thickener in various cleaning applications. It is formulated for use in gels, osmotic pump tablets, and conventional tablets, offering water solubility for effective performance.

IFF Pharma SolutionsMETHOCEL™ K200M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Suspension
Labeling Claims:Sugar-free, Low Odor, Palm Oil-free, Dioxin-free, Pesticide-free, APE-free, Kosher, Endocrine Disruptor-free, Odor-free, Vegan, PAH-free, Natural Latex Rubber-Free, Antibiotics-free, Dye Free, PFAS-Free, Colorants-free, CMR Substances-free, USP 232 Elemental Impurities Free, TSE-free, Paraben-free, Triphenyl Tin Compounds-Free, BSE-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Halal, Bisphenol A-free, PVC-free, Vegetarian, Naturally Derived, Hormones-free, Zero Calorie, Plasticizer-free, Hypoallergenic, Perfluorooctanoic Acid-free, Mycotoxins-free, Aflatoxin-free, Aluminum-free, Phthalates-free, PFOS-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, British Pharmacopeia (BP), JECFA (FAO/WHO), GMP, FDA 21 CFR 172.874, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Halal, Kosher, EU Packaging Directive (94/62/EC), Swiss Ordinance (SR 817.023.21), CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), WEEE Directive 2012/19/EU, FEMA Compliant, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), National Formulary (NF), European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1169/2011, FCC Compliant, National Bioengineered Food Disclosure Standard, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, EXCiPACT, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, ISO 14001
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K200M Premium CR HPMC used in ceramics and pharmaceuticals, acts as a binder and enables immediate release in suspensions and tablet coatings. It also serves as a film former, gelling agent, mucoadhesive, and solubilizer, offering versatile applications due to its water solubility.

IFF Pharma SolutionsAccelerate® DS - 812

Chemical Name:Croscarmellose Sodium, Cellulose Gum
Dosage Form:Tablets, Capsules, Granules, Soft Chews, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Palm Oil-free, GMO-free, Dioxin-free, Pesticide-free, APE-free, Endocrine Disruptor-free, Odor-free, Ethylene Oxide-free, Vegan, PAH-free, Natural Latex Rubber-Free, Antibiotics-free, Dye Free, PFAS-Free, Nanomaterials-free, Colorants-free, TSE-free, Paraben-free, Triphenyl Tin Compounds-Free, BSE-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, Glycerin-free, Melamine-free, Bisphenol A-free, PVC-free, Vegetarian, Hormones-free, Plasticizer-free, Perfluorooctanoic Acid-free, Non-GMO, Impurities-free, Not Listed In California Proposition 65, Aluminum-free, Phthalates-free, PFOS-free, Tributyl Tin Compounds-Free, Sugar-free
Certifications & Compliance:Nagoya Compliant, Regulation (EU) No. 1272/2008, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ICH Q3C, FDA 21 CFR Regulations
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.

IFF Pharma SolutionsETHOCEL™ Standard 7 Premium Ethylcellulose

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

ETHOCEL™ Standard 7 Premium Ethylcellulose White Powder has binding, controlled release, flexibility, and thermal stability benefits. It's soluble in organic solvents and ethanol. Used in direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating. It functions as a controlled release agent, granulation aid, and taste masking agent.

IFF Pharma SolutionsPOLYOX™ WSR - 303 LEO NF Grade HV Select

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Dosage Form:Tablets, Gels, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules
Labeling Claims:Residual Solvent -Free, Ethylene Glycol-free, Not Tested on Animals, Pesticide-free, Fungicide-free, Allergen-free, Vegetarian, Diethylene Glycol-free, Vegan, Chlorine-free, Dairy-free, Gluten-free, Not Listed In California Proposition 65, Nitrosamines-free, Herbicide-free
Certifications & Compliance:British Pharmacopeia (BP), Belgian Law And Codex Alimentarius Standards, Chinese Pharmacopeia (ChP), GMP, FDA Compliant, ICH Q3C, United States Pharmacopeia (USP), EXCiPACT, Clean Water Act (CWA) Certified, Japan Pharmacopeia (JP), National Formulary (NF), European Pharmacopeia (Ph. Eur.)

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.

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