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IFF Pharma Solutions
Accelerate® 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.
IFF Pharma Solutions
METHOCEL™ F4M HPMC - Specialty
Functions:
Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Binder, Emulsifier
Chemical Name:
Hydroxypropyl Methylcellulose
Chemical Family:
Cellulose & Cellulosics, Cellulose Ethers
Dosage Form:
Tablets
Certifications & Compliance:
Regulation (EC) No. 1333/2008, cGMP, 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, FSC Certified, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), EU Cosmetic Regulation 1223/2009 Compliant, 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, Nagoya Compliant, 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)
Features:
Cold Water Dispersible, Improved Dispersion, High Cohesion, Low Surface Tension, Improved Adhesion, Water Soluble, Good Gelling Behaviour, Non-Toxic, Non-Ionic, Good Thickening Properties, Anti-settling Properties, Low Ash Content, Thixotropic, Good pH Stability, Wide pH Range
METHOCEL™ F4M HPMC - Specialty a cellulose ether commonly known as hypromellose, acts as a rheology modifier, ensuring consistent performance. With certifications such as CMR substance-free, dairy-free, diethylene glycol-free, dioxane-free, and dye-free, it guarantees safety and purity in formulations.
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