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Pharmaceutical Actives & Precursors

Excipients

Pharmaceutical Actives & Precursors

167 Products found on IFF Pharma Solutions in Pharmaceuticals & Nutraceuticals

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IFF Pharma SolutionsCELSENTIAL™ E6 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
Functions:Viscosity Modifier
CAS Number:9004-65-3
Labeling Claims:Odor-free, Halal, TSE-free, CMR Substances-free, Endocrine Disruptor-free, Kosher, Not Listed In California Proposition 65, BSE-free
Certifications & Compliance:FDA 21 CFR 172.874, Directive 2002/95/EC, IFANCA Halal, ISO 9001, United States Pharmacopeia (USP), Kosher, Directive 2011/65/EU (RoHS 2), Directive 2001/83/EC, Directive 1333/2008/EC, GMP, Turkish RoHS Regulation, Directive 2023/2055/EU, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), ICH Q3C, Indian Pharmacopeia

CELSENTIAL™ E6 Premium LV HPMC, a cellulose ether identified as hypromellose, is an efficient viscosity modifier. It's certified BSE-free, CMR substance-free, and endocrine disruptor-free, ensuring safety and regulatory compliance in diverse applications.

IFF Pharma SolutionsCELSENTIAL™ E15 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
Functions:Viscosity Modifier
CAS Number:9004-65-3
Labeling Claims:Odor-free, Halal, TSE-free, CMR Substances-free, Endocrine Disruptor-free, Kosher, BSE-free
Certifications & Compliance:FDA 21 CFR 172.874, Directive 2002/95/EC, IFANCA Halal, ISO 9001, United States Pharmacopeia (USP), Kosher, 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, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), ICH Q3C, Indian Pharmacopeia

CELSENTIAL™ E15 Premium LV HPMC, recognised as a cellulose ether, specifically hypromellose, is proficient as a viscosity modifier. This product boasts certifications affirming its freedom from BSE and CMR substances, ensuring safety and compliance with stringent regulatory standards.

IFF Pharma SolutionsAc-Di-Sol® SD - 711

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Orally Disintegrating Tablets (ODTs), Capsules, Granules
Labeling Claims:Generally Recognized As Safe (GRAS), Vegan, Kosher, BSE-free, Non-GMO, Halal, TSE-free, Vegetarian, Pareve
Certifications & Compliance:EC No.1907/2006, Halal, Japan Pharmacopeia (JP), National Formulary (NF), FSSC 22000, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), IFANCA Halal, EXCiPACT, ISO 9001, Kosher
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.

IFF Pharma SolutionsMETHOCEL™ E3 Premium LV HPMC

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Tablets, Suspension
Ingredient Origin:Plant Origin
Labeling Claims:Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, Hypoallergenic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, VOC-free, TSE-free, Pareve, Perfluorooctanoic Acid-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, USP 232 Elemental Impurities Free, Mycotoxins-free, Kosher, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, APE-free, Odor-free, Pesticide-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan, Low Odor

METHOCEL™ E3 Premium LV HPMC suitable for suspensions, offers binding properties crucial for ceramic applications. With granulation and tablet coating manufacturing technologies, it ensures efficient production processes. Additionally, its water solubility makes it ideal for pharmaceutical and nutraceutical applications, serving as a binder and controlled release agent.

IFF Pharma SolutionsViscarin® PH - 209NF

Chemical Name:Carrageenan
CAS Number:9000-07-1
Dosage Form:Soft Gels
Labeling Claims:Monosodium Glutamate (MSG)-free, PFOS-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Antibiotics-free, Colorants-free, Dioxin-free, Animal Products-free, GMO-free, Natural Latex Rubber-Free, COSMOS Approved, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Organic, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free
Certifications & Compliance:EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA 21 CFR 177.1520, European Commission Decision 97/534/EC, European Pharmacopeia (Ph. Eur.), FDA 21 CFR 179.26, Regulation (EU) No. 1829/2003, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, ISO 9001, Regulation (EU) No. 1830/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FDA 7 CFR 205.605, Orthodox Union Kosher, ABNT NBR 14725, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, 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.

IFF Pharma SolutionsAvicel® CL - 611

Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
Dosage Form:Spray, Suspension
Labeling Claims:Triphenyl Tin Compounds-Free, Genotoxic-free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Melamine-free, Colorants-free, Amine-free, Latex-free, Dioxin-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Not Tested on Animals, Tributyl Tin Compounds-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Perfluorooctanoic Acid-free, Glycerin-free
Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), Kosher, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Japanese Pharmaceutical Excipients (JPE), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher
Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression

Avicel® CL - 611 a non-animal-origin ingredient, is used in sprays and suspensions. It's compatible with various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceuticals, it acts as a binder, filler, stabilizer, and immediate release agent. It's also an emulsifying agent and viscosity modifier, aiding suspension.

IFF Pharma SolutionsPOLYOX™ WSR - N10 LEO NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
Manufacturing Technology:Direct Compression

POLYOX™ WSR - N10 LEO NF Grade an off-white powder, is prized for its water solubility, making it an effective binder and thickener in both cleaning and cosmetic products. Its versatility and solubility make it a valuable ingredient for various formulations.

IFF Pharma SolutionsProtanal® HF120 RBS

Chemical Name:Sodium Alginate
Labeling Claims:Halal, Paraben-free, Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP)
Chemical Inventories:PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China)

Protanal® HF120 RBS derived from non-animal sources, is potassium alginate, functioning as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceuticals and nutraceuticals. It is available in powder form.

IFF Pharma SolutionsProtanal® LF - MG 5/60

Chemical Name:Magnesium Alginate
Labeling Claims:Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free, Halal, Paraben-free
Certifications & Compliance:IFRA Compliant, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008
Chemical Inventories:AICS (Australia), NDSL (Canada), DSL (Canada)

Protanal® LF - MG 5/60 is a non-animal origin powder serving multiple functions in pharmaceuticals and nutraceuticals. It acts as an antacid, controlled release agent, gelling agent, and stabilizer, providing versatile benefits for various formulations.

IFF Pharma SolutionsPRONOVA® SLM20

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Biodegradable, Halal
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® SLM20 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™ K100M Premium HPMC

INCI Name:Methylcellulose
Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Tablets
Ingredient Origin:Plant Origin
Labeling Claims:Natural Latex Rubber-Free, Dioxin-free, Vegetarian, Tributyl Tin Compounds-Free, Vegan, Low Odor, Non-GMO, Palm Oil-free, Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, USP 232 Elemental Impurities Free, Mycotoxins-free, Kosher, Preservative-free, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Halal, Hypoallergenic, Hormones-free, PVC-free, Naturally Derived, Organic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, APE-free, Pesticide-free, Triphenyl Tin Compounds-Free, Generally Recognized As Safe (GRAS), CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Plasticizer-free, VOC-free, Irradiation-free, TSE-free, Glycerin-free, Pareve, Sugar-free, PFOS-free, Perfluorooctanoic Acid-free, BSE-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based

METHOCEL™ K100M Premium HPMC is employed in ceramics as a binder, utilizing granulation in its manufacturing process. Within pharmaceuticals and nutraceuticals, it serves as a suspension aid, thickener, and viscosity modifier, boasting water solubility for versatile application.

IFF Pharma SolutionsProtanal® CR - 8133

Chemical Name:Sodium Alginate
Labeling Claims:Halal, Paraben-free, Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free
Certifications & Compliance:Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP)

Protanal® CR - 8133 featuring sodium alginate, serves various functions in pharmaceuticals and nutraceuticals. It acts as controlled release agent, emulsifying agent, gelling agent, thickener, and viscosity modifier, available in powder form.

IFF Pharma SolutionsETHOCEL™ Standard 14 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Functions:Controlled Release Agent, Granulation Aid, Binder, Taste Masker
Dosage Form:Tablets
Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, GMO-free, Sewage Sludge Free, Plasticizer-free
Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), FDA 21 CFR 573.420, European Regulation 396/2005/EC, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, EC No. 1935/2004, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Encapsulation, Direct Compression

ETHOCEL™ Standard 14 Premium Ethylcellulose available in powder form, is adaptable for various manufacturing processes such as direct compression, encapsulation, and granulation. It exhibits ethanol solubility, offering versatility in pharmaceutical and industrial applications.

IFF Pharma SolutionsPRONOVA® SLG100

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Biodegradable, Halal
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® SLG100 offers dosage forms as foams with labeling claims for high purity and biodegradability. It finds markets in healthcare and pharmaceuticals for drug delivery and care solutions, particularly in topical applications, and in printing and packaging for inkjet printing. Its functions include serving as an encapsulant and gelling agent.

IFF Pharma SolutionsManugel® DMB

Chemical Name:Sodium Alginate
Labeling Claims:Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free, Halal, Paraben-free, Formaldehyde-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, Aflatoxin-free, Copper-free, PFOS-free, Residual Solvent -Free, Heavy Metal-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Antibiotics-free, Melamine-free, Barium-free, Cadmium-free, Colorants-free, Latex-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free
Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), EU Cosmetic Regulation 1223/2009 Compliant, 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.

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