Drug Delivery & Care Solutions

130 Products found in Drug Delivery & Care Solutions

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Oral

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 SolutionsPOLYOX™ WSR - 303 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 - 303 LEO NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.

IFF Pharma SolutionsMETHOCEL™ K100 Premium LV DC2 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, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, 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, Regulation (EU) No. 2022/1396, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Directive 2023/915/EU
Manufacturing Technology:Granulation, Direct Compression

METHOCEL™ K100 Premium LV DC2 HPMC widely used in pharmaceuticals, serves as a controlled release agent and film former. Its formulation facilitates direct compression and granulation, making it suitable for various dosage forms, like suspensions and tablet coatings. Additionally, its water solubility enhances its effectiveness in diverse applications.

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 SolutionsETHOCEL™ Standard 10 HP Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Labeling Claims:Odor-free, Quaternary Ammonium Salt-Free, Phthalates-free, Kosher, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Dye Free, 1,4-Dioxane-free, PFOA-free, Antibiotics-free, Bisphenol Derivatives-free, Sugar-free, PVC-free, Gluten-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Dioxane-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Vegetarian, FSSC 22000, Non-Irritant, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Non-Mutagenic, Iodide-free, Potassium-free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), JECFA (FAO/WHO), Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, RoHS Compliant, EuPIA Listed, EFSA (European Food Safety Authority) Certified, EXCiPACT, FDA 21 CFR 172.868, CFDA Compliant (China), RoHS 2 Compliant, Directive 2011/65/EU (RoHS 2), United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), FSC Certified, European Pharmacopeia (Ph. Eur.), Directive 2012/19/EU, ISO 9000, Regulation (EU) No. 1169/2011, FCC Compliant, Turkish RoHS Regulation, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, FDA 21 CFR 73.1001, FDA Compliant, Hazard Analysis Critical Control Point (HACCP), Directive 1333/2008/EC, Regulation (EU) No. 231/2012, ICH Q3C, GMP, FDA 21 CFR 117, National Formulary (NF), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Belgian Law And Codex Alimentarius Standards, ICH Q3D
Manufacturing Technology:Tablet Coating, Granulation

ETHOCEL™ Standard 10 HP Premium Ethylcellulose is ideal for phenolics, modified rosins, alkyds (Long Oil), and fluid bed coating applications. Notable features include excellent adhesion, good green strength, high gloss, good printability, and reduced tack, ensuring superior performance and finish in industrial processes.

IFF Pharma SolutionsManucol® LMT2

Chemical Name:Sodium Alginate
Labeling Claims:Dioxin-free, Gold-Free, Phthalates-free, Cadmium-free, 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), ABNT NBR 14725, 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.), 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® LMT2 is free from caffeine, colorants, dioxins, dyes, hormones, MSG, and natural latex rubber. It functions as an antacid, controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical formulations.

IFF Pharma SolutionsPOLYOX™ WSR - N60K LEO NF Grade

Chemical Name:Polyethylene Oxide, Pyrogenic Silica
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, 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 - N60K LEO NF Grade an off-white powder, offers versatile applications. Its industrial additives function as binders and thickeners, aiding in direct compression manufacturing. In pharmaceuticals, it acts as a binder and controlled release agent. Soluble in water, it suits abuse deterrent tablets & capsules, gels, and osmotic pump tablets.

IFF Pharma SolutionsSeaGel® CAP - 201

Chemical Name:Carrageenan
Functions:Encapsulant, Controlled Release Agent
Labeling Claims:Environmentally Friendly, Potassium-free, Dye Free, Plasticizer-free, PHO (Partially Hydrogenated Oil)-Free, Kosher, Paraben-free, PFAS-Free, Antibiotics-free, Aluminum-free, Plant-Based, Sustainable, Pesticide-free, PVC-free, Not Listed In California Proposition 65, Non-GMO, Vegetarian, Generally Recognized As Safe (GRAS), Iodide-free, Nitrosamines-free, Naturally Derived, Caffeine Free, Bisphenol Derivatives-free, Clean Label, Allergen-free, Fungicide-free, PFOS-free, Sugar-free, Hormones-free, Dioxane-free, Natural, APE-free, Natural Latex Rubber-Free, Quaternary Ammonium Salt-Free, Halal, Phthalates-free, Doping Substances-free, PFOA-free, BSE-free, Herbicide-free, Vegan, Preservative-free, Glycerin-free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Palm Oil-free, PAH-free, Gluten-free, Monosodium Glutamate (MSG)-free
Certifications & Compliance:Regulation (EU) No. 1272/2008, Clean Water Act (CWA) Certified, Nagoya Compliant
Dosage Form:Capsules

SeaGel® CAP - 201 identified as carrageenan, offers versatility and quality in capsule applications. With its natural and non-animal plant origins, it ensures ethical sourcing. Featuring easy-to-use powder form, it boasts film-forming properties, heat, and thermal stability. Additionally, it functions as an encapsulant and controlled release agent, providing enhanced performance in encapsulation processes.

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 SolutionsAlubra® PG - 100

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

Alubra® PG - 100 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.

Sodium Hyaluronate Pharma Grade - 80 banner

IFF Pharma SolutionsSodium Hyaluronate Pharma Grade - 80

Chemical Name:Sodium Hyaluronate
Functions:Anti-Adhesion Promoter
CAS Number:9067-32-7
Labeling Claims:High Purity
Certifications & Compliance:Certificates of Suitability (CEP), US DMF
Dosage Form:Eye Drops

Sodium Hyaluronate Pharma Grade - 80 a versatile solution suitable for various applications. With its chemical name, sodium hyaluronate, it's designed for use in eye drops, delivering reliable performance. It's renowned for its high purity and serves as an effective anti-adhesion promoter in pharmaceutical and nutraceutical formulations.

IFF Pharma SolutionsMETHOCEL™ E6 Premium LV Capsule Grade HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Capsules, Suspension, Tablets
Labeling Claims:Low Odor, Quaternary Ammonium Salt-Free, Dioxin-free, Phthalates-free, No Artificial Sweeteners, Colorants-free, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, 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, 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, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Hypoallergenic, PFOS-free, Naturally Derived, PFAS-Free, Impurities-free, Fungicide-free, PAH-free, Plant-Based, Radioactive-free, Potassium-free
Certifications & Compliance:Halal, REACH Exempt (Europe), British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), FCC Compliant, Regulation (EC) No. 1333/2008, FDA Compliant, Directive 1333/2008/EC, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, Regulation (EU) No. 2022/1396, GMP, National Formulary (NF), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA
Manufacturing Technology:Tablet Coating, Granulation, Wet Granulation

METHOCEL™ E6 Premium LV Capsule Grade HPMC is a versatile product with various applications and functions. Ideal for tablet coating, granulation, wet granulation, tablets, and capsules, it ensures controlled and immediate release. Free from sewage sludge, it serves as a thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive, making it indispensable in pharmaceutical and nutraceutical formulations. Suitable for food containers and packaging, it boasts water solubility, ensuring quality performance in suspension formulations.

IFF Pharma SolutionsPOLYOX™ WSR - 303 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 - 303 NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.

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 SolutionsEndurance® VE - 102

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, 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 - 102 comprising microcrystalline cellulose, finds applications in dietary supplements. It functions as a binder in food and nutrition, as well as in pharmaceuticals and nutraceuticals, presenting as a powder.

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