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IFF Pharma Solutions

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Excipients

Pharmaceutical Actives & Precursors

Nutraceuticals & Supplements

189 Products found on IFF Pharma Solutions in Pharmaceuticals & Nutraceuticals

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TDSWith TDS

IFF Pharma SolutionsAquateric® N100

Dosage Form:Tablets, Capsules
Labeling Claims:Kosher, Non-GMO
Certifications & Compliance:Kosher

Aquateric® N100 available in powder form, is suitable for various dosage forms, such as capsules and tablets, particularly in dietary supplements. It serves as a release agent in food applications and offers the benefit of being non-GMO. Utilized in tablet coating manufacturing technology, it functions as an enteric coating system and an extended-release agent in pharmaceutical and nutraceutical products.

IFF Pharma SolutionsManucol® LB

Chemical Name:Sodium Alginate
Labeling Claims:Odor-free, Dioxin-free, Gold-Free, Phthalates-free, Cadmium-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dye Free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Bisphenol A-free, Barium-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Cobalt-free
Certifications & Compliance:British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Japan Pharmacopeia (JP), Belgian Law And Codex Alimentarius Standards
Chemical Inventories:PICCS (Phillipines), AICS (Australia), KECI (Korea), ENCS (Japan), IECSC (China), NDSL (Canada), DSL (Canada)

Manucol® LB containing sodium alginate, is a versatile ingredient known for its antacid properties. It also acts as a controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical formulations.

IFF Pharma SolutionsAvicel® PH - 103

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Granules, Suspension, Tablets
Labeling Claims:Fragrance allergen-free, Quaternary Ammonium Salt-Free, BSE-free, Phthalates-free, Kosher, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, 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, Ethylene Oxide-free, Latex-free, APE-free, Hormones-free, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Fungicide-free, PAH-free, Iodide-free, Potassium-free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA Compliant, ICH Q3C, FDA 21 CFR 117, Nagoya Compliant, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Belgian Law And Codex Alimentarius Standards
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

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.

IFF Pharma SolutionsLattice® NT-50

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Functions:Binder
Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Dye Free, Pesticide-free, Allergen-free, Aluminum-free, Natural Latex Rubber-Free, Kosher, PFAS-Free, Preservative-free, PFOS-free, Halal, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Not Listed In California Proposition 65, Hormones-free, Sugar-free, Tributyl Tin Compounds-Free, Antibiotics-free, BSE-free, PVC-free, PAH-free, Phthalates-free, Triphenyl Tin Compounds-Free, Caffeine Free, TSE-free, Plasticizer-free, APE-free, Latex-free, Non-GMO
Certifications & Compliance:ICH Q3C, FDA Food Safety Modernization Act (FSMA), United States Pharmacopeia (USP), cGMP, Generally Recognized As Safe (GRAS), Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), Clean Water Act (CWA) Certified

Lattice® NT-50 an off-white product, is available as granules and tablets. It's caffeine-free, colorant-free, dioxin-free, and dye-free, meeting diverse preferences. A trusted binder in pharmaceutical and nutraceutical applications, it's provided in powder form for easy use.

IFF Pharma SolutionsProtanal® Ester K3B426

Chemical Name:Propyleneglycol alginate
CAS Number:9005-37-2
Labeling Claims:Dioxin-free, BSE-free, Gold-Free, Phthalates-free, Cadmium-free, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Barium-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Residual Solvent -Free, Cobalt-free, Solvent-free
Certifications & Compliance:British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Japan Pharmacopeia (JP)

Protanal® Ester K3B426 ensures peace of mind with its labeling claims of being free from bisphenol A, caffeine, colorants, and dioxin. This versatile powder serves multiple functions in pharmaceuticals, belonging to both excipients and active pharmaceutical ingredients (APIs) categories.

IFF Pharma SolutionsETHOCEL™ Standard 4 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, 1,4-Dioxane-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, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Formaldehyde-free, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, Halal, British Pharmacopeia (BP), Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, RoHS Compliant, Swiss Ordinance (SR 817.023.21), EuPIA Listed, EXCiPACT, FDA 21 CFR 172.868, CFDA Compliant (China), RoHS 2 Compliant, Doping-Free, United States Pharmacopeia (USP), FDA 21 CFR 181.24, WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Japan Chemical Substances Control Law (CSCL), Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FCC Compliant, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, FDA 21 CFR 73.1001, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 573.420, ICH Q3C, Canadian Environmental Protection Act (CEPA), National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, ICH Q3D
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Direct Compression, Encapsulation

ETHOCEL™ Standard 4 Premium Ethylcellulose is a white powder that is soluble in ethanol and organic solvents. It provides benefits such as binding, controlled release, excellent flexibility, and thermal stability, making it highly suitable for various industrial applications where these properties are critical.

IFF Pharma SolutionsMETHOCEL™ K15M Premium CR HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Suspension
Labeling Claims:Low Odor, Odor-free, 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, EU Packaging Directive (94/62/EC), British Pharmacopeia (BP), JECFA (FAO/WHO), ABNT NBR 14725, 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), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K15M Premium CR HPMC suitable for ceramics and pharmaceuticals, functions as a binder and enables controlled release in suspensions and tablet coatings. Its water solubility enhances efficacy, and it serves as a film former, gelling agent, and mucoadhesive, broadening its utility.

IFF Pharma SolutionsPOLYOX™ WSR - N750 LEO 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 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.

IFF Pharma SolutionsETHOCEL™ Standard 10 FP Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, 1,4-Dioxane-free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, CMR Substances-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Formaldehyde-free, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, British Pharmacopeia (BP), Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, RoHS Compliant, Swiss Ordinance (SR 817.023.21), EuPIA Listed, EXCiPACT, FDA 21 CFR 172.868, CFDA Compliant (China), RoHS 2 Compliant, Doping-Free, United States Pharmacopeia (USP), FDA 21 CFR 181.24, WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Japan Chemical Substances Control Law (CSCL), Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FCC Compliant, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, FDA 21 CFR 73.1001, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 573.420, ICH Q3C, Canadian Environmental Protection Act (CEPA), National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, ICH Q3D
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Direct Compression, Encapsulation

ETHOCEL™ Standard 10 FP Premium Ethylcellulose a white powder, boasts various benefits such as binding, controlled release, excellent flexibility, and thermal stability. It is manufactured using techniques like direct compression, encapsulation, granulation, and hot melt extrusion. Additionally, it exhibits solubility in ethanol and organic solvents.

IFF Pharma SolutionsPOLYOX™ WSR - 301 LEO 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 - 301 LEO 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.

IFF Pharma SolutionsPOLYOX™ WSR - N10 LEO 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 - 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 SolutionsETHOCEL™ Standard 20 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, 1,4-Dioxane-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, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Formaldehyde-free, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, Halal, British Pharmacopeia (BP), Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, RoHS Compliant, Swiss Ordinance (SR 817.023.21), EuPIA Listed, EXCiPACT, FDA 21 CFR 172.868, CFDA Compliant (China), RoHS 2 Compliant, Doping-Free, United States Pharmacopeia (USP), FDA 21 CFR 181.24, WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Japan Chemical Substances Control Law (CSCL), Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, FCC Compliant, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, FDA 21 CFR 73.1001, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 573.420, ICH Q3C, Canadian Environmental Protection Act (CEPA), National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, ICH Q3D
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Direct Compression, Encapsulation

ETHOCEL™ Standard 20 Premium Ethylcellulose White powder for binding, controlled release, flexibility, and thermal stability. Ideal for hot melt coating tablets, it is soluble in organic solvents and ethanol. It aids in granulation and acts as a taste masking agent. Suitable for direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating.

IFF Pharma SolutionsKelset® NF

Chemical Name:Sodium Alginate
Functions:Controlled Release Agent

Kelset® NF, available in a convenient powder form, is a member of the alginate chemical family. Its versatility and reliability make it a preferred choice for various applications. With its unique properties and chemical composition, Kelset® NF ensures consistent performance and ease of use in diverse industrial processes. Whether in food, pharmaceuticals, or other sectors, this product stands out for its quality and effectiveness.

IFF Pharma SolutionsGelcarin® GP - 812

Chemical Name:Carrageenan
CAS Number:9000-07-1
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-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, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-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), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Japan Pharmacopeia (JP)
Manufacturing Technology:Encapsulation

Gelcarin® GP - 812 composed of carrageenan, is manufactured using encapsulation technology. It serves multiple functions in pharmaceuticals and nutraceuticals, including as a controlled-release agent, emulsifying agent, gelling agent, stabilizer, and thickener.

IFF Pharma SolutionsManucol® LKX

Chemical Name:Sodium Alginate
Dosage Form:Suspension, Tablets
Labeling Claims:Dioxin-free, Gold-Free, Phthalates-free, Cadmium-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dye Free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Bisphenol A-free, Barium-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Cobalt-free
Certifications & Compliance:British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Japan Pharmacopeia (JP), Belgian Law And Codex Alimentarius Standards
Chemical Inventories:PICCS (Phillipines), AICS (Australia), ENCS (Japan), IECSC (China), NDSL (Canada), DSL (Canada), ECL (Korea)

Manucol® LKX serves as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical applications, available in both suspension and tablet forms.

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