Products

IFF Pharma Solutions

2 Products found on IFF Pharma Solutions  in Base Fluids, Glidants & Lubricants

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POLYOX™ WSR - N12K FP NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K FP NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Kosher, Vegan, TSE-free, Diethylene Glycol-free, Fungicide-free, Pesticide-free, Allergen-free, Residual Solvent -Free, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, Herbicide-free, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free, Gluten-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, EC No. 1935/2004, ISO 9001, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, FFDCA, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
POLYOX™ WSR - N12K FP NF Grade composed of ethylene oxide copolymers and polyethylene oxide, serves diverse functions in pharmaceutical formulations. It finds application in abuse-deterrent tablets and capsules, gels, osmotic pump tablets, and regular tablets. This versatile ingredient acts as a binder, thickener, and controlled release agent, ensuring optimal performance. Available in powder form, it demonstrates water solubility, facilitating easy integration into formulations for enhanced effectiveness.
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Alubra® PG - 100 banner
IFF Pharma SolutionsAlubra® PG - 100
  • Chemical Name:Sodium Stearyl Fumarate
  • Dosage Form:Tablets, Capsules
  • Labeling Claims:Endocrine Disruptor-free, PVC-free, Hormones-free, Phthalates-free, Colorants-free, PFOS-free, Paraben-free, Natural Latex Rubber-Free, Triphenyl Tin Compounds-Free, Ethylene Oxide-free, Perfluorooctanoic Acid-free, PHO (Partially Hydrogenated Oil)-Free, Preservative-free, Plasticizer-free, Tributyl Tin Compounds-Free, PAH-free, Pesticide-free, Nitrosamines-free, Bisphenol A-free, Dioxin-free, Caffeine Free, Antibiotics-free, Amine-free, Sugar-free, APE-free, Dye Free, PFAS-Free, Aluminum-free, Monosodium Glutamate (MSG)-free
  • Certifications & Compliance:FDA Compliant, FCC Compliant, Doping-Free, Japan Pharmacopeia (JP), United States Pharmacopeia (USP), British Pharmacopeia (BP), EXCiPACT, EC No.1907/2006, National Formulary (NF), European Pharmacopeia (Ph. Eur.)
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.
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