Products

IFF Pharma Solutions

21 Products found on IFF Pharma Solutions in Other Excipients

SDSWith SDS

TDSWith TDS

Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
Dosage Form:Suspension, Lotions, Spray
Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Ethylene Oxide-free, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Mercury-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, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Zinc-free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), Japanese Pharmaceutical Excipients (JPE), JECFA (FAO/WHO), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, 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), ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003, IFANCA Halal, IFRA Compliant
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® RC - 591 is versatile, catering to various dosage forms like lotions, sprays, and suspensions. Its manufacturing technology involves direct compression, dry granulation, and wet granulation methods. In pharmaceutical and nutraceutical applications, it serves as a binder, compression aid, immediate release agent, and stabilizer, ensuring product efficacy and stability.

IFF Pharma SolutionsPRONOVA® UP MVG

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Halal, Biodegradable
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® 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 SolutionsAvicel® PH - 302

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, ABNT NBR 14725, 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 - 302 identified as microcrystalline cellulose, is a cornerstone in pharmaceutical applications such as granules, suspensions, and tablets. Its versatility encompasses direct compression, dry granulation, and wet granulation processes. Functioning as a binder, compression aid, filler, and immediate release agent, Avicel® PH - 302 ensures robust formulations and consistent performance across diverse pharmaceutical products.

IFF Pharma SolutionsPRONOVA® UP LVG

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Halal, Biodegradable
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® UP LVG 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 SolutionsPRONOVA® UP LVM

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Halal, Biodegradable
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® UP LVM 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 SolutionsGelcarin® PH - 812

Chemical Name:Carrageenan
CAS Number:9000-07-1
Labeling Claims:Vegan, Bisphenol Derivatives-free, Fragrance allergen-free, Diethylene Glycol-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, PVC-free, Hormones-free, Fungicide-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, Herbicide-free, APE-free, Caffeine Free, Iodide-free, Dye Free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, PAH-free, PFOS-free, Antibiotics-free, Allergen-free, Non-GMO, Paraben-free, Sugar-free, Aluminum-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Phthalates-free, Pesticide-free, PFOA-free, Kosher, Dioxane-free, Preservative-free, PFAS-Free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), Kosher, FDA 21 CFR 117, Halal, National Formulary (NF), Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), Nagoya Compliant, FSSC 22000
Manufacturing Technology:Encapsulation

Gelcarin® PH - 812 is optimized for encapsulation, serving as a controlled release agent, emulsifying agent, gelling agent, stabilizer, and thickener. Identified as a polysaccharide, specifically carrageenan, it ensures reliable performance in various formulations.

IFF Pharma SolutionsAvicel® PH - 200

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Tablets
Labeling Claims:Not Tested on Animals, Ethylene Oxide-free, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-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, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, Heavy Metal-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, 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), 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, IFRA Compliant
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® PH - 200 composed of microcrystalline cellulose, finds application in tablet formulations. Manufactured using direct compression, dry granulation, and wet granulation techniques, it serves as a binder and compression aid. Derived from non-animal sources, it meets pharmaceutical and nutraceutical standards.

IFF Pharma SolutionsAvicel® PH - 113

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Tablets
Labeling Claims:Not Tested on Animals, Ethylene Oxide-free, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-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, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, Heavy Metal-free, PFAS-Free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, 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), 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, IFRA Compliant
Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation

Avicel® PH - 113 composed of microcrystalline cellulose, finds application in tablet formulations. Manufactured using direct compression, dry granulation, and wet granulation techniques, it serves as a binder and compression aid. Derived from non-animal sources, it meets pharmaceutical and nutraceutical standards.

IFF Pharma SolutionsPRONOVA® SLG20

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, 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® SLG20 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 SolutionsPRONOVA® SLM100

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Halal, Biodegradable
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® 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 SolutionsPRONOVA® UP MVM

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Biocompatible, High Purity, Halal, Biodegradable
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® 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 SolutionsPRONOVA® UP VLVG

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

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Controlled Release Agent, Coating System, Binder, Thickener, Solubilizer, Film Former
Dosage Form:Capsules, Tablets, Suspension, Orally Disintegrating Films (ODFs), Granules
Labeling Claims:Sewage Sludge Free, Odor-free, Quaternary Ammonium Salt-Free, Halal, Tributyltin (TBT) - Free, USP 232 Elemental Impurities Free, Paraben-free, Gluten-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Perfluorocarbon (PFC)-free, Bisphenol A-free, Glycerin-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Herbicide-free, Palm Oil-free, Solvent-free, Pesticide-free, No Artificial Sweeteners, Low Aldehyde, Diethylene Glycol-free, Irradiation-free, Nitrosamines-free, PFAS-Free, Impurities-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, NPE-free, CMR Substances-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, FSSC 22000, Steroids Free, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Residues-free, Allergen-free, Vegan, Antibiotics-free, Radioactive-free, Kosher, Ethylene Glycol-free, Fungicide-free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Bactericide-free, Organic, Colorants-free, Plant-Based, PVC-free, Non-Toxic, VOC-free, Persistent Organic Pollutants (POP)-free, Potassium-free
Certifications & Compliance:Japan Pharmacopeia (JP), FDA 21 CFR 174.5, JECFA (FAO/WHO), EC No. 2023/2006, SCF Listed, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Directive 1333/2008/EC, 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, EU Cosmetic Regulation 1223/2009 Compliant, European Parliament and Council Directive (E464), FDA 21 CFR 176.170, Regulation (EU) No. 1935/2004, National Formulary (NF), FDA 21 CFR 175.300, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, Kosher, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, FDA 21 CFR 176.180, EC No. 1935/2004, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, FDA 21 CFR 175.105, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Directive 2012/19/EU, Regulation (EU) No. 1169/2011, FCC Compliant, Regulations (EU) No. 1129/2011, USDA Organic, EXCiPACT, Directive 2011/62/EU, EFSA (European Food Safety Authority) Certified, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), EU Directive 2002/72/EC, cGMP
Manufacturing Technology:Tablet Coating, Wet Granulation

METHOCEL™ VLV Premium HPMC is a versatile industrial additive designed for various applications, including tablet coating, orally disintegrating films, capsules, suspensions, and granules. With high efficiency and water solubility, it offers excellent cohesion development, green strength, and water retention. It functions as a binder, emulsifier, lubricant, and surfactant make it indispensable across manufacturing processes. Additionally, it serves as a water retention agent, binder and resin, slip agent, coating system, mucoadhesive, film former, viscosity modifier, solubilizer, gelling agent, and immediate release agent. METHOCEL™ VLV Premium HPMC's improved pumpability and lubricating properties ensure easy handling, making it a go-to choice for industrial and pharmaceutical formulations.

IFF Pharma SolutionsAvicel® PH - 112

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, ABNT NBR 14725, 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 - 112 is used in direct compression, dry granulation, and wet granulation applications. It is caffeine-free, CMR substance-free, diethylene glycol-free, and dioxane-free, ensuring safe and effective pharmaceutical formulations.

IFF Pharma SolutionsPRONOVA® SLG100

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Kosher, Not Listed In California Proposition 65, Biocompatible, High Purity, Halal
Certifications & Compliance:Clean Water Act (CWA) Certified, ISO 14001, National Formulary (NF), SARA 311/312, Hazard Analysis Critical Control Point (HACCP), European Pharmacopeia (Ph. Eur.), ISO 9000, SARA 313, Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), United States Pharmacopeia (USP), GMP, Directive 2023/2055/EU, EC No.1907/2006
Manufacturing Technology:Encapsulation

PRONOVA® SLG100 is available in the form of foams. It serves as an encapsulant and gelling agent. The product is offered in powder and solid forms, catering to various pharmaceutical and nutraceutical applications, including emulsifiers and stabilizers and modified and controlled-release excipients.

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