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225 Products found on IFF Pharma Solutions

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METHOCEL™ E6 Premium LV Capsule Grade HPMC banner
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.
Avicel® PH - 112 banner
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.
METHOCEL™ K100 Premium LVCR HPMC banner
IFF Pharma SolutionsMETHOCEL™ K100 Premium LVCR 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, Regulation (EU) No. 2022/1396, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ K100 Premium LVCR HPMC belonging to the cellulose ether chemical family, is manufactured using granulation technology. In pharmaceuticals and nutraceuticals, it serves as a controlled release agent, film former, gelling agent, immediate release agent, and mucoadhesive, offering water solubility for diverse applications.
ETHOCEL™ Standard 10 Premium Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Standard 10 Premium Ethylcellulose - Specialty
  • INCI Name:Ethylcellulose
  • Ingredient Name:Ethyl Cellulose
  • Chemical Family:Cellulose Ethers, Cellulose & Cellulosics
  • Ingredient Origin:Plant Origin
  • Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Paraben-free, Dye Free, GMO-free, Allergen-free, Aluminum-free, Natural Latex Rubber-Free, Kosher, Preservative-free, PFOS-free, Palm Oil-free, Hormones-free, Aflatoxin-free, Sugar-free, Antibiotics-free, Glycerin-free, BSE-free, Phthalates-free, Plant-Based, Mycotoxins-free, Plasticizer-free, Colorants-free, Naturally Derived, Vegan, Pesticide-free, Formaldehyde-free, PFAS-Free, Halal, Dioxin-free, CMR Substances-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Nitrosamines-free, Endocrine Disruptor-free, Tributyl Tin Compounds-Free, Zero Calorie, PVC-free, 1,4-Dioxane-free, PAH-free, Triphenyl Tin Compounds-Free, Caffeine Free, TSE-free, APE-free, Vegetarian
  • Certifications & Compliance:Clean Air Act (CAA) Certified, Regulation (EC) No. 1333/2008, Regulation (EU) No. 231/2012, Chinese Pharmacopeia (ChP), ICH Q3C, CFDA Compliant (China), FDA Compliant, EXCiPACT, Canadian Environmental Protection Act (CEPA), Indian Pharmacopeia, National Formulary (NF), United States Pharmacopeia (USP), EuPIA Listed, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FDA 21 CFR 181.24, Regulation (EU) No. 10/2011 (PIM), FCC Compliant, European Regulation 396/2005/EC, Halal, Kosher, Doping-Free, Japan Chemical Substances Control Law (CSCL), WEEE Directive 2012/19/EU, Directive 2023/915/EU, EU Cosmetic Regulation 1223/2009 Compliant, FDA 21 CFR 172.868, Regulation (EU) No. 1169/2011, European Pharmacopeia (Ph. Eur.), RoHS 2 Compliant, FDA 21 CFR 573.420, Majelis Ulama Indonesia Halal, ICH Q3D, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, cGMP, Turkish RoHS Regulation, FDA 21 CFR 73.1, FDA 21 CFR 163, Belgian Law And Codex Alimentarius Standards, FDA 21 CFR 73.1001, RoHS Compliant, Swiss Ordinance (SR 817.023.21)
ETHOCEL™ Standard 10 Premium Ethylcellulose - Specialty characterized by its white color, serves as a stabilizer and thickener in cosmetic ingredients. Utilizing encapsulation, granulation, hot melt extrusion, and tablet coating technologies, it is available in a powdered physical form.
Accelerate® DS - 813 banner
IFF Pharma SolutionsAccelerate® DS - 813
  • Chemical Name:Cellulose Gum
  • Functions:Disintegrant
  • Manufacturing Technology:Wet Granulation
  • Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Vegan, Dye Free, Pesticide-free, GMO-free, Allergen-free, Aluminum-free, Generally Recognized As Safe (GRAS), Natural Latex Rubber-Free, PFAS-Free, Preservative-free, PFOS-free, Nanomaterials-free, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Not Listed In California Proposition 65, Palm Oil-free, Hormones-free, Melamine-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, Ethylene Oxide-free, Non-GMO, Vegetarian
  • Certifications & Compliance:Regulation (EU) No. 231/2012, ICH Q3C, European Pharmacopeia (Ph. Eur.), Nagoya Compliant, FDA 21 CFR Regulations, FDA Food Safety Modernization Act (FSMA), United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, cGMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), European Regulation 396/2005/EC, Doping-Free
Accelerate® DS - 813 is available in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs). Manufactured using wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical formulations. It is supplied in powder form for ease of processing and formulation.

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