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216 Products found on IFF Pharma Solutions

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IFF Pharma SolutionsPOLYOX™ WSR 303 - Specialty

Chemical Name:Pyrogenic Silica, Polyethylene Oxide, Polyethylene Glycol
Polymer Name:Polyethylene Glycol
CAS Number:25322-68-3
Chemical Family:Polyethers, Polyethylene Glycols, Ethylene Oxide Copolymers, Polyglycols, Non-Ionics

POLYOX™ WSR 303 - Specialty a white powder, is used in gels, osmotic pump tablets, and regular tablets. It offers viscoelasticity, lubricity, and a silky feel, making it suitable for sprayers, tissue, and toweling. It's water-soluble, compatible with polystyrene and polycaprolactone, and non-toxic.

IFF Pharma SolutionsAccelerate® DS - 812

Chemical Name:Croscarmellose Sodium, Cellulose Gum
Dosage Form:Orally Disintegrating Tablets (ODTs), Granules, Soft Chews, Tablets, Capsules
Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Melamine-free, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, PFOS-free, Antibiotics-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, Vegetarian, TSE-free, Impurities-free, Palm Oil-free, Phthalates-free, Pesticide-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
Certifications & Compliance:Doping-Free, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), FDA 21 CFR Regulations, Nagoya Compliant, FSSC 22000, Orthodox Union Kosher, IFANCA Halal
Manufacturing Technology:Wet Granulation

Accelerate® DS - 812 contains cellulose gum and is available in capsule, granule, and orally disintegrating tablet forms. Utilizing wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical applications.

ETHOCEL™ Standard 6 Industrial Ethylcellulose - Specialty banner

IFF Pharma SolutionsETHOCEL™ Standard 6 Industrial Ethylcellulose - Specialty

Ingredient Name:Ethyl Cellulose
Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Chemical Family:Cellulose Ethers, Cellulose & Cellulosics
Pigment Type:Metallic Effect
Dosage Form:Tablets
Labeling Claims:Natural Latex Rubber-Free, Organic, Allergen-free, Dioxane-free, Antibiotics-free, Hormones-free, Dairy-free, Zero Calorie, Monosodium Glutamate (MSG)-free, Phthalates-free, Paraben-free, Non-Mutagenic, Non-Irritant, Preservative-free, PHO (Partially Hydrogenated Oil)-Free, APE-free, Non-GMO, Dye Free, Aluminum-free, Sewage Sludge Free, Potassium-free, PFOA-free, PVC-free, Pesticide-free, FSSC 22000, Sugar-free, Iodide-free, 1,4-Dioxane-free, Nitrosamines-free, Gluten-free, Quaternary Ammonium Salt-Free, Plasticizer-free, Halal, PFOS-free, Bisphenol Derivatives-free, Caffeine Free, Irradiation-free, Odor-free, VOC-free, PFAS-Free, Kosher, Tributyltin (TBT) - Free, PAH-free
Color (Properties):White
Certifications & Compliance:FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), EC No. 1935/2004, EU Cosmetic Regulation 1223/2009 Compliant, ISO 9000, Directive 2012/19/EU, Regulation (EU) No. 1272/2008, Directive 2009/48/EC, Halal, European Regulation 396/2005/EC, Regulation (EU) No. 1169/2011, FDA 21 CFR 73.1001, Japan Pharmacopeia (JP), FDA 21 CFR 101.9, EC No. 2023/2006, EC No.1907/2006, National Formulary (NF), Chinese Pharmacopeia (ChP), ICH Q3C, EU Directive 2002/72/EC, EFSA (European Food Safety Authority) Certified, RoHS Compliant, Indian Pharmacopeia, FCC Compliant, Belgian Law And Codex Alimentarius Standards, FDA 21 CFR 73.1, Kosher, ISO 9001, Organic Certified, Regulation (EU) No. 10/2011 (PIM), British Pharmacopeia (BP), GMP, Directive 1333/2008/EC, Directive 2011/65/EU (RoHS 2), FDA 21 CFR 117, FSSC 22000, United States Pharmacopeia (USP), FDA Compliant, EuPIA Listed, Regulation (EU) No. 231/2012, USDA Organic, Regulation (EC) No. 1333/2008, FSC Certified, JECFA (FAO/WHO), cGMP, FDA 21 CFR 172.868, RoHS 2 Compliant, Turkish RoHS Regulation, Hazard Analysis Critical Control Point (HACCP)
Manufacturing Technology:Encapsulation, Granulation, Tablet Coating, Direct Compression

ETHOCEL™ Standard 6 Industrial Ethylcellulose - Specialty excels in granulation, tablet coating, spray, and phenolics applications. With attributes like good green strength, high gloss, printability, and reduced tack, it ensures superior performance. Acting as a controlled release agent, granulation aid, taste masking agent, rheology modifier, and binder & resin, it's available in powder or granule form, organic solvent soluble, and white in color for compatibility with diverse industrial needs.

METHOCEL™ 311 Powder HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ 311 Powder HPMC - Specialty

Functions:Binder, Emulsifier, Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal)
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:Tablets
Certifications & Compliance:ISO 9001, Directive 1333/2008/EC, FDA 21 CFR 101.9, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), FSSC 22000, Generally Recognized As Safe (GRAS), RoHS Compliant, RoHS 2 Compliant, Regulation (EC) No. 1333/2008, cGMP, Majelis Ulama Indonesia Halal, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), ISO 50001, Organic Certified, Chinese Pharmacopeia (ChP), Regulation (EU) No. 2022/1396, European Pharmacopeia (Ph. Eur.), USDA Organic, FDA 21 CFR 182.1480, FFDCA, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), European Regulation 396/2005/EC, EU Cosmetic Regulation 1223/2009 Compliant, Doping-Free, Clean Air Act (CAA) Certified, Turkish RoHS Regulation, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1830/2003, Directive 2009/48/EC, United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, Orthodox Union Kosher, Regulation (EU) No. 1272/2008
Features:Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range, Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties

METHOCEL™ 311 Powder HPMC - Specialty (hydroxypropyl methylcellulose), is classified under the chemical family of cellulose ethers, specifically known as hypromellose. It functions as a rheology modifier and is sourced from plants, available in powdered physical form.

IFF Pharma SolutionsAlubra® PG - 100

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

IFF Pharma SolutionsAlubra® PG - 30

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

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