Protanal® Ester K3B426 ensures peace of mind with its labeling claims of being free from bisphenol A, caffeine, colorants, and dioxin. This versatile powder serves multiple functions in pharmaceuticals, belonging to both excipients and active pharmaceutical ingredients (APIs) categories.
Chemical Name: Propyleneglycol alginate
CAS Number: 9005-37-2
Labeling Claims: APE-free, Aflatoxin-free, Allergen-free, Aluminum-free, Animal Products-free, Antibiotics-free, BSE-free, Barium-free, Bisphenol A-free, Cadmium-free, Caffeine Free, Cobalt-free, Colorants-free, Copper-free, Dioxin-free, Dye Free, Endocrine Disruptor-free, Ethylene Oxide-free, GMO-free, Generally Recognized As Safe (GRAS), Glycerin-free, Gold-Free, Halal, Hormones-free, Irradiation-free, Kosher, Latex-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Mycotoxins-free, Nanomaterials-free, Natural Latex Rubber-Free, Nitrosamines-free, Non-GMO, PAH-free, PFAS-Free, PFOS-free, PHO (Partially Hydrogenated Oil)-Free, PVC-free, Palm Oil-free, Paraben-free, Pareve, Perfluorooctanoic Acid-free, Pesticide-free, Phthalates-free, Plasticizer-free, Preservative-free, Propylene Glycol-free, Residual Solvent -Free, Solvent-free, Sugar-free, TSE-free, Tributyl Tin Compounds-Free, Triphenyl Tin Compounds-Free, Vegetarian
Certifications & Compliance: British Pharmacopeia (BP), Doping-Free, EC No. 2023/2006, EC No.1907/2006, EU Cosmetic Regulation 1223/2009 Compliant, EU Packaging Directive (94/62/EC), EXCiPACT, European Pharmacopeia (Ph. Eur.), European Regulation 396/2005/EC, FCC Compliant, FDA Compliant, FDA Food Safety Modernization Act (FSMA), FSSC 22000, GMP, Generally Recognized As Safe (GRAS), Halal Food Council of Europe, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant, ISO 14001, ISO 9000, ISO 9001, JECFA (FAO/WHO), Japan Pharmacopeia (JP), Kosher, National Formulary (NF), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1829/2003, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, Regulation (EU) No. 231/2012, United States Pharmacopeia (USP)
