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130 Products found on IFF Pharma Solutions in Drug Delivery & Care Solutions

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IFF Pharma SolutionsPRONOVA® UP MVM

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
Manufacturing Technology:Encapsulation

PRONOVA® UP MVM 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 SolutionsPOLYOX™ N60K LEO NF HV

Chemical Name:Polyethylene Oxide, Pyrogenic Silica, Polyethylene Glycol
CAS Number:25322-68-3
Dosage Form:Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules, Tablets, Gels
Labeling Claims:Chlorine-free, Ethylene Glycol-free, Not Tested on Animals, Allergen-free, Vegetarian, Vegan, Dairy-free, Herbicide-free, Nitrosamines-free, Fungicide-free, Diethylene Glycol-free, Gluten-free, Pesticide-free, Residual Solvent -Free
Certifications & Compliance:British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), FDA Compliant, EXCiPACT, ICH Q3C, United States Pharmacopeia (USP), National Formulary (NF), EC No.1907/2006, Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), Belgian Law And Codex Alimentarius Standards

POLYOX™ N60K LEO NF HV containing polyethylene oxide (PEG-45M) serves multiple functions in various applications. Its versatility extends to deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. Functioning as a thickener, binder, and controlled release agent, it ensures optimal formulation performance. Available in powder form, it exhibits water solubility, enhancing its usability in diverse pharmaceutical formulations.

IFF Pharma SolutionsPRONOVA® UP VLVM

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
Manufacturing Technology:Encapsulation

PRONOVA® UP VLVM 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 SolutionsPOLYOX™ WSR - N12K FP NF Grade

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

POLYOX™ WSR - N12K FP NF Grade 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 SolutionsViscarin® PH - 109NF

Chemical Name:Carrageenan
CAS Number:9000-07-1
Dosage Form:Soft Gels
Labeling Claims:Triphenyl Tin Compounds-Free, Plasticizer-free, Dioxin-free, Monosodium Glutamate (MSG)-free, BSE-free, Generally Recognized As Safe (GRAS), Caffeine Free, Phthalates-free, Preservative-free, Colorants-free, Glycerin-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegetarian, Bisphenol A-free, Vegan, APE-free, Hormones-free, Dye Free, GMO-free, Natural Latex Rubber-Free, TSE-free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Antibiotics-free, Palm Oil-free, Sugar-free, Non-GMO, PFAS-Free, PAH-free, PVC-free, Aluminum-free, Tributyl Tin Compounds-Free, Pesticide-free, Paraben-free
Certifications & Compliance:Regulation (EU) No. 1169/2011, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, ABNT NBR 14725, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Regulation (EU) No. 231/2012, Doping-Free, European Regulation 396/2005/EC, National Formulary (NF), European Pharmacopeia (Ph. Eur.)
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 SolutionsPOLYOX™ WSR N 80NF TG LEO

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

POLYOX™ WSR N 80NF TG LEO, in an off-white powder form, serves as a binder and thickener in cleaning and pharmaceutical formulations. Its water solubility makes it suitable for various applications, while its direct compression manufacturing technology ensures efficient production processes. Additionally, it functions as a controlled release agent, adding value to pharmaceutical formulations.

IFF Pharma SolutionsPRONOVA® UP MVG

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
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.

IFF Pharma SolutionsViscarin® GP109

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

Viscarin® GP109 with encapsulation manufacturing, caters to drug delivery and oral care solutions in healthcare and pharma markets. It acts as an encapsulant, gelling agent, and stabilizer, offering versatility in formulation and processing aids within pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsPRONOVA® SLM100

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
Manufacturing Technology:Encapsulation

PRONOVA® SLM100 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 SolutionsMETHOCEL™ F4M Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Labeling Claims:Low Odor, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, CMR Substances-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, REACH Exempt (Europe), EU Packaging Directive (94/62/EC), British Pharmacopeia (BP), JECFA (FAO/WHO), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, Swiss Ordinance (SR 817.023.21), EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, FEMA Compliant, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, National Formulary (NF), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU
Manufacturing Technology:Granulation

METHOCEL™ F4M Premium HPMC is water-soluble and finds application in ceramics and pharmaceuticals. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, suspension aid, thickener, and viscosity modifier. Produced through granulation, it serves various industrial and pharmaceutical functions.

IFF Pharma SolutionsEndurance® VE - 101

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Functions:Binder
Manufacturing Technology:Wet Granulation, Direct Compression
Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Dye Free, Pesticide-free, GMO-free, Allergen-free, Aluminum-free, Generally Recognized As Safe (GRAS), Natural Latex Rubber-Free, Kosher, PFAS-Free, Preservative-free, PFOS-free, Halal, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Palm Oil-free, Hormones-free, Endocrine Disruptor-free, Sugar-free, Tributyl Tin Compounds-Free, Antibiotics-free, Glycerin-free, BSE-free, PVC-free, PAH-free, Phthalates-free, Triphenyl Tin Compounds-Free, Caffeine Free, TSE-free, Plasticizer-free, APE-free, Latex-free, Ethylene Oxide-free, Non-GMO
Certifications & Compliance:Regulation (EU) No. 231/2012, ICH Q3C, European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), National Formulary (NF), United States Pharmacopeia (USP), cGMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FCC Compliant, European Regulation 396/2005/EC, Halal, Doping-Free

Endurance® VE - 101 containing microcrystalline cellulose, is utilized in dietary supplements for its binding properties. It serves as a binder in both food and pharmaceutical applications, providing structural integrity in powder form.

IFF Pharma SolutionsPOLYOX™ WSR - 1105 NF Grade

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

POLYOX™ WSR - 1105 NF Grade an off-white powder, serves as a binder and thickener in cleaning agents. It is available in powder form and is water-soluble, making it suitable for use in gels and osmotic pump tablets.

IFF Pharma SolutionsMETHOCEL™ K200M Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Capsules, Suspension, Tablets
Labeling Claims:Low Odor, Odor-free, Quaternary Ammonium Salt-Free, BSE-free, Phthalates-free, Kosher, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dairy-free, Persistent Organic Pollutants (POP)-free, Dye Free, Herbicide-free, TSE-free, PFOA-free, Antibiotics-free, Bisphenol Derivatives-free, Palm Oil-free, Sugar-free, PVC-free, Diethylene Glycol-free, Gluten-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, CMR Substances-free, Dioxane-free, Plasticizer-free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Latex-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Fungicide-free, PAH-free, Iodide-free, Pareve, Potassium-free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), Waste Electrical & Electronic Equipment Directive (WEEE), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA 21 CFR 176.170, FDA Food Safety Modernization Act (FSMA), Kosher, Swiss Ordinance (SR 817.023.21), EXCiPACT, FDA 21 CFR 175.300, United States Pharmacopeia (USP), FDA 21 CFR 174.5, Regulation (EU) No. 10/2011 (PIM), FSC Certified, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA Compliant, ICH Q3C, GMP, Nagoya Compliant, FDA 21 CFR 175.105, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FDA 21 CFR 176.180, Belgian Law And Codex Alimentarius Standards
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K200M Premium HPMC, identified as cellulose ethers and hypromellose, serves a wide array of functions across capsules, suspensions, tablets, granulation, and tablet coating applications. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, thickener, and viscosity modifier. Notably, it is water-soluble, ensuring versatility and efficacy in formulations.

IFF Pharma SolutionsAc-Di-Sol® SDW - 802

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Capsules, Granules, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Odor-free, Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Nanomaterials-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:Halal, British Pharmacopeia (BP), China DMF, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, Nagoya Compliant, National Formulary (NF), FDA 21 CFR Regulations, Japan Pharmacopeia (JP)
Manufacturing Technology:Wet Granulation

Ac-Di-Sol® SDW - 802 is a versatile ingredient suitable for capsules, granules, and orally disintegrating tablets (ODTs). Employing wet granulation, it serves as a disintegrant and immediate release agent in pharmaceutical and nutraceutical formulations.

IFF Pharma SolutionsPOLYOX™ WSR - N750 NF Grade

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

POLYOX™ WSR - N750 NF Grade is available in various dosage forms including gels, osmotic pump tablets, and traditional tablets. Utilizing direct compression manufacturing technology, it serves applications in both oral and topical drug delivery within the healthcare and pharmaceutical markets. With its properties as a binder and thickener, this white, water-soluble powder aids in formulation processes.

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