Other Excipients

21 Products found in Other Excipients

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:High Purity, Biocompatible
Certifications & Compliance: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 SolutionsAvicel® PH - 302

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), ABNT NBR 14725, 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 - 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 SolutionsGelcarin® GP - 911

Chemical Name:Carrageenan
CAS Number:9000-07-1
Labeling Claims:Ethylene Glycol-free, Fragrance allergen-free, Monosodium Glutamate (MSG)-free, BSE-free, Kosher, Endocrine Disruptor-free, Allergen-free, Vegetarian, Vegan, Ethylene Oxide-free, Herbicide-free, TSE-free, Non-GMO, Fungicide-free, Diethylene Glycol-free, Gluten-free, Pesticide-free, Halal, CMR Substances-free
Certifications & Compliance:Halal, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, Doping-Free, FDA 21 CFR 117, United States Pharmacopeia (USP), Nagoya Compliant, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), European Pharmacopeia (Ph. Eur.), Belgian Law And Codex Alimentarius Standards
Manufacturing Technology:Encapsulation

Gelcarin® GP - 911 is ideal for encapsulation applications, acting as a controlled release agent, emulsifying agent, gelling agent, stabilizer, and thickener. Identified as a polysaccharide, it ensures efficient performance in various formulations.

IFF Pharma SolutionsPRONOVA® UP VLVG

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 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
Dosage Form:Orally Disintegrating Films (ODFs), Capsules, Granules, Suspension, Tablets
Labeling Claims:APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Naturally Derived, PFAS-Free, Impurities-free, Fungicide-free, PAH-free, Plant-Based, Radioactive-free, Potassium-free, Solvent-free, Low Odor, Odor-free, Quaternary Ammonium Salt-Free, Dioxin-free, Phthalates-free, No Artificial Sweeteners, Kosher, Colorants-free, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Residues-free, Persistent Organic Pollutants (POP)-free, Herbicide-free, PFOA-free, Antibiotics-free, Palm Oil-free, Sugar-free, Low Aldehyde, PVC-free, Diethylene Glycol-free, Gluten-free, Aluminum-free, NPE-free, Pesticide-free, Steroids Free, Paraben-free, Non-Toxic, Halal, Bactericide-free, CMR Substances-free, Plasticizer-free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Perfluorocarbon (PFC)-free, Preservative-free, Glycerin-free, Artificial Flavor-Free, Vegetarian, Bisphenol A-free, FSSC 22000
Certifications & Compliance:Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, GMP, FDA 21 CFR 175.105, National Formulary (NF), European Parliament and Council Directive (E464), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA, FDA 21 CFR 176.180, Regulations (EU) No. 1129/2011, Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, SCF Listed, cGMP, Halal, REACH Exempt (Europe), British Pharmacopeia (BP), JECFA (FAO/WHO), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA 21 CFR 176.170, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EFSA (European Food Safety Authority) Certified, EXCiPACT, CFDA Compliant (China), FDA 21 CFR 175.300, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 1935/2004, FDA 21 CFR 174.5, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Directive 2012/19/EU, Regulation (EU) No. 1169/2011, FCC Compliant, EC No. 2023/2006, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Directive 2011/62/EU, Directive 1333/2008/EC
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 SolutionsPRONOVA® SLM20

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® 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 SolutionsPRONOVA® SLG100

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® 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 SolutionsGelcarin® GP - 379

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 - 379 derived from carrageenan of non-animal origin, serves various pharmacological and nutraceutical functions, including being a controlled-release agent, emulsifying agent, gelling agent, stabilizer, and thickener.

IFF Pharma SolutionsAvicel® PH - 112

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), ABNT NBR 14725, 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 - 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 SolutionsAlubra® PG - 30

Chemical Name:Sodium Stearyl Fumarate
CAS Number:4070-80-8
Dosage Form:Tablets
Labeling Claims:Plasticizer-free, Dioxin-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Phthalates-free, Preservative-free, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, Dye Free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Antibiotics-free, Sugar-free, PFAS-Free, PAH-free, PVC-free, Aluminum-free, Tributyl Tin Compounds-Free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free
Certifications & Compliance:FCC Compliant, REACH Exempt (Europe), British Pharmacopeia (BP), FDA Compliant, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), National Formulary (NF), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.)

Alubra® PG - 30 is available in both capsule and tablet forms, making it versatile for pharmaceutical applications. It meets labeling claims for being caffeine-free and free of colorants. In pharmaceutical and nutraceutical functions, it acts as an immediate release agent and a lubricant, aiding in the manufacturing process.

IFF Pharma SolutionsAvicel® PH - 200

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-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, 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, Latex-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, Heavy Metal-free, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, 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.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS)
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

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 SolutionsGelcarin® PH - 812

Chemical Name:Carrageenan
CAS Number:9000-07-1
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, 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, Vegetarian, Ethylene Oxide-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: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, 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: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 SolutionsPRONOVA® UP LVM

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 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 SolutionsPRONOVA® UP LVG

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 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 SolutionsAvicel® RC - 591

Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
Dosage Form:Lotions, Suspension, Spray
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-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, 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, Latex-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Japanese Pharmaceutical Excipients (JPE), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, GMP, National Formulary (NF), Generally Recognized As Safe (GRAS)
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

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.

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