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202 Products found on IFF Pharma Solutions

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POLYOX™ WSR Coagulant LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant 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 Coagulant LEO NF Grade is an off-white to white powder that is water soluble. It is used in dosage forms such as abuse deterrent tablets, capsules, and gels, providing essential properties for these pharmaceutical applications.
Protanal® SF - 80 M banner
IFF Pharma SolutionsProtanal® SF - 80 M
  • Chemical Name:Sodium Alginate
  • Ingredient Name:Sodium Alginate
  • CAS Number:9005-38-3
  • Labeling Claims:PVC-free, Melamine-free, Gold-Free, PFAS-Free, Potassium-free, Impurities-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, NPE-free, CMR Substances-free, Plasticizer-free, Nanomaterials-free, Copper-free, Barium-free, APE-free, Quaternary Ammonium Salt-Free, Vegetarian, Residual Solvent -Free, Halal, Tributyltin (TBT) - Free, Paraben-free, Gluten-free, Cadmium-free, Propylene Glycol-free, PAH-free, Steroids Free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Caffeine Free, Tin-free, Perfluorocarbon (PFC)-free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, Latex-free, Radioactive-free, Aflatoxin-free, TSE-free, Mercury-Free, Herbicide-free, Kosher, Animal Products-free, Fungicide-free, Hormones-free, BSE-free, Palm Oil-free, Solvent-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Bactericide-free, No Artificial Sweeteners, Colorants-free, Irradiation-free, Cobalt-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), GMP, Generally Recognized As Safe (GRAS), cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FFDCA, JECFA (FAO/WHO), EC No. 2023/2006, Kosher, European Regulation 396/2005/EC, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, FDA 21 CFR 117, European Pharmacopeia (Ph. Eur.), IFRA Compliant, EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), ISO 14001, Regulation (EU) No. 1829/2003, Halal Food Council of Europe, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ISO 9000, EXCiPACT
  • Chemical Inventories:AICS (Australia), NDSL (Canada), ECL (Korea), PICCS (Phillipines), ENCS (Japan), IECSC (China), DSL (Canada)
Protanal® SF - 80 M is a versatile powder ideal for pharmaceuticals and nutraceuticals. Free from sewage sludge, it serves as a controlled release agent, gelling agent, thickener, stabilizer, and antacid, ensuring optimal performance in various applications.
SeaGel® CAP - 101 banner
IFF Pharma SolutionsSeaGel® CAP - 101
  • Chemical Name:Carrageenan
  • Functions:Encapsulant, Controlled Release Agent
  • Labeling Claims:Organic, Paraben-free, Phthalates-free, Tributyl Tin Compounds-Free, Triphenyl Tin Compounds-Free, Non-GMO, Dye Free, GMO-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Environmentally Friendly, Natural, Aluminum-free, PAH-free, TSE-free, Sustainable, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Palm Oil-free, Dioxin-free, APE-free, Preservative-free, Kosher, Bisphenol A-free, Sugar-free, Hormones-free, Naturally Derived, PFAS-Free, Vegetarian, Perfluorooctanoic Acid-free, Nitrosamines-free, Antibiotics-free, Animal Products-free, Plasticizer-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free
  • Certifications & Compliance:Directive 1333/2008/EC, Regulation (EU) No. 1829/2003, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, European Regulation 396/2005/EC, FSSC 22000, ISO 9001, cGMP, Halal, EU Cosmetic Regulation 1223/2009 Compliant, Doping-Free, Regulation (EU) No. 1272/2008, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1169/2011, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Directive 396/2005/EC, FDA 21 CFR 177.1520, Orthodox Union Kosher, FDA 21 CFR 179.26, IFRA Compliant
  • 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.
Avicel® PH - 103 banner
IFF Pharma SolutionsAvicel® PH - 103
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Granules, Tablets, Suspension
  • Labeling Claims:Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Not Tested on Animals, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Genotoxic-free, Ethylene Glycol-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, PAH-free, Free of Major Allergens, 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, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Kosher, Amine-free, Dioxane-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Potassium-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Orthodox Union Kosher, Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003, IFANCA Halal
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
Avicel® PH - 103 is a microcrystalline cellulose used in direct compression, dry granulation, and wet granulation technologies. It serves the healthcare and pharma markets, particularly in oral drug delivery and care solutions. This product is available in granule form.
METHOCEL™ E50 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ E50 Premium LV HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Lubricant (Internal), Surfactant, Emulsifier, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Sustained Release Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Binder, Thickener, Film Former, Solubilizer, Film Former
  • Dosage Form:Tablets, Suspension
  • Labeling Claims:Dye Free, Sewage Sludge Free, Odor-free, Triphenyl Tin Compounds-Free, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Mycotoxins-free, Pareve, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Aflatoxin-free, BSE-free, Palm Oil-free, Pesticide-free, Irradiation-free, Perfluorooctanoic Acid-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Allergen-free, Vegan, Not Listed In California Proposition 65, Hypoallergenic, Antibiotics-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, PVC-free, VOC-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, National Formulary (NF), Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, European Regulation 396/2005/EC, ICH Q3C, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP)
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ E50 Premium LV HPMC is a versatile ingredient suitable for various applications. In suspension dosage forms, it serves as a binder for ceramics, while its granulation and tablet coating manufacturing technologies make it adaptable for different production processes. With properties such as film formation, gelling, and mucoadhesion, it functions in pharmaceutical and nutraceutical applications, facilitating immediate release and solubilization when needed.
Endurance® VE - 102 banner
IFF Pharma SolutionsEndurance® VE - 102
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Functions:Binder
  • Manufacturing Technology:Direct Compression, Wet Granulation
  • Labeling Claims:Dye Free, Plasticizer-free, APE-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Ethylene Oxide-free, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Solvent-free, Not Tested on Animals, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free, PFAS-Free, Zinc-free, Aluminum-free, Endocrine Disruptor-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Kosher, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), ISO 45001, ISO 14001, Orthodox Union Kosher, National Formulary (NF), FCC Compliant, ISO 22000, Generally Recognized As Safe (GRAS)
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.
METHOCEL™ F4M Modified Cellulose Food Grade - Specialty banner
IFF Pharma SolutionsMETHOCEL™ F4M Modified Cellulose Food Grade - Specialty
  • Ingredient Name:Hydroxypropyl Methyl Cellulose (HPMC)
  • Chemical Name:Hydroxypropyl Methylcellulose
  • Ingredient Origin:Plant Origin
  • Functions:Controlled Release Agent, Viscosity Modifier, Thickener, Film Former, Binder
  • Labeling Claims:Dye Free, Sewage Sludge Free, Odor-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Mycotoxins-free, Pareve, Dairy-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Aflatoxin-free, BSE-free, Palm Oil-free, Pesticide-free, Irradiation-free, Perfluorooctanoic Acid-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Vegan, Hypoallergenic, Antibiotics-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, PVC-free, VOC-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), FDA 21 CFR 174.5, JECFA (FAO/WHO), EC No. 2023/2006, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, Directive 1333/2008/EC, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, ISO 50001, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 176.170, Regulation (EU) No. 1935/2004, National Formulary (NF), FDA 21 CFR 175.300, Directive 2001/83/EC, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Doping-Free, FDA 21 CFR 176.180, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, FDA 21 CFR 175.105, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1169/2011, FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), Directive 2023/2055/EU
  • Physical Form:Powder
  • Dosage Form:Tablets
METHOCEL™ F4M Modified Cellulose Food Grade - Specialty known for its water solubility, is utilized in various pharmaceutical and nutraceutical applications. It serves as a controlled release agent, film former, and gelling agent. Its manufacturing involves granulation and tablet coating processes.
POLYOX™ WSR - N12K NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K 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 - N12K 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.
POLYOX™ WSR - 301 FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 301 FP 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 - 301 FP 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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