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IFF Pharma Solutions
POLYOX™ WSR - 1105 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 - 1105 NF Grade an off-white powder, serves as a binder and thickener in cleaning agents. It is available in powder form and is water-soluble, making it suitable for use in gels and osmotic pump tablets.
IFF Pharma Solutions
POLYOX™ WSR - 205 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 - 205 LEO NF Grade is an off-white powder used as a binder and thickener in cleaning ingredients and pharmaceuticals. It functions in various dosage forms, including tablets, gels, and osmotic pump tablets, utilizing direct compression technology. It offers water solubility.
IFF Pharma Solutions
METHOCEL™ E50 Premium LV HPMC - Specialty
Functions:
Binder, Thickener, Processing Aid
Chemical Family:
Cellulose & Cellulosics, Cellulose Ethers
End Uses:
Ceramics
METHOCEL™ E50 Premium LV HPMC - Specialty is a versatile ingredient suitable for various applications. In suspension dosage forms, it serves as a binder for ceramics, while its granulation and tablet coating manufacturing technologies make it adaptable for different production processes. With properties such as film formation, gelling, and mucoadhesion, it functions in pharmaceutical and nutraceutical applications, facilitating immediate release and solubilization when needed.
IFF Pharma Solutions
ETHOCEL™ Standard 200 Industrial Ethylcellulose - Specialty
Chemical Family:
Cellulose Ethers, Cellulose & Cellulosics
Labeling Claims:
Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, 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, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Formaldehyde-free, Tributyl Tin Compounds-Free
Certifications & Compliance:
cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, 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, 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, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Regulation (EU) No. 231/2012, ICH Q3C, Canadian Environmental Protection Act (CEPA), Japan Pharmacopeia (JP), Directive 2023/915/EU, ICH Q3D
ETHOCEL™ Standard 200 Industrial Ethylcellulose - Specialty a white powder, boasts versatile applications. It excels in binding and controlled release, offering flexibility and thermal stability. Additionally, it serves as a stabilizer and thickener in cosmetic formulations, soluble in ethanol.
IFF Pharma Solutions
Endurance® VE - 090
Chemical Name:
Cellulose, Microcrystalline
CAS Number:
9004-34-6
Dosage Form:
Tablets
Labeling Claims:
Aluminum-free, Tributyl Tin Compounds-Free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Odor-free, Plasticizer-free, Dioxin-free, Monosodium Glutamate (MSG)-free, BSE-free, Generally Recognized As Safe (GRAS), Caffeine Free, Phthalates-free, Preservative-free, Kosher, Colorants-free, Glycerin-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Bisphenol A-free, Ethylene Oxide-free, Latex-free, APE-free, Hormones-free, Dye Free, GMO-free, Natural Latex Rubber-Free, TSE-free, Perfluorooctanoic Acid-free, PFOS-free, Antibiotics-free, Palm Oil-free, Sugar-free, Non-GMO, PFAS-Free, PAH-free, PVC-free
Certifications & Compliance:
Generally Recognized As Safe (GRAS), FCC Compliant, cGMP, Halal, FDA Food Safety Modernization Act (FSMA), Kosher, Regulation (EU) No. 231/2012, ICH Q3C, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC
Manufacturing Technology:
Wet Granulation, Direct Compression
Endurance® VE - 090 is used in dietary supplements, functioning as a binder. It comes with labeling claims of being aluminum-free, antibiotic-free, APE-free, and bisphenol-A-free. Additionally, it serves as a binder in pharmaceuticals and nutraceuticals.
IFF Pharma Solutions
Avicel® RC - 581
Chemical Name:
Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
CAS Number:
9004-34-6
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, 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® RC - 581 consisting of microcrystalline cellulose, is produced using direct compression, dry granulation, and wet granulation technologies. It serves various functions in pharmaceuticals and nutraceuticals, acting as a compression aid, filler, and immediate release agent.
IFF Pharma Solutions
Avicel® DG
Chemical Name:
Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
CAS Number:
9004-34-6
Dosage Form:
Tablets
Labeling Claims:
Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-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, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, Latex-free, APE-free, Hormones-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:
cGMP, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC 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® DG derived from non-animal sources, is a versatile powder used in tablet manufacturing. Its chemical composition includes calcium, hydrogen phosphate, cellulose, and cellulosics. Employing direct compression or wet granulation techniques, it functions as a binder and compression aid in tablet formulations.
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