Labeling Claims Pvc Free - IFF Pharma Solutions - page 15

215 Products found on IFF Pharma Solutions

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IFF Pharma SolutionsProtanal® LF - 10/60B

Chemical Name:Sodium Alginate
Labeling Claims:Steroids Free, No Artificial Sweeteners, Colorants-free, Copper-free, Natural Latex Rubber-Free, Naturally Derived, Halal, BSE-free, PVC-free, Hormones-free, Fungicide-free, Glycerin-free, Plasticizer-free, Quaternary Ammonium Salt-Free, Gluten-free, NPE-free, Pareve, Herbicide-free, Solvent-free, Perfluorocarbon (PFC)-free, Mycotoxins-free, Residual Solvent -Free, APE-free, Caffeine Free, Plant-Based, Barium-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Cobalt-free, Gold-Free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, CMR Substances-free, PHO (Partially Hydrogenated Oil)-Free, Tributyltin (TBT) - Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Impurities-free, Cadmium-free, Palm Oil-free, Bactericide-free, Phthalates-free, Pesticide-free, Animal Products-free, PFOA-free, Radioactive-free, GMO-free, Kosher, Tin-free, Preservative-free, PFAS-Free, Conflict minerals-free, Nanomaterials-free, Potassium-free, Vegan
Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), GMP, Kosher, FDA 21 CFR 117, Doping-Free, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FFDCA, FDA Food Safety Modernization Act (FSMA), Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), IFRA Compliant

Protanal® LF- 10/60B is a versatile powder designed for pharmaceutical and nutraceutical applications. It serves as a controlled-release agent, gelling agent, thickener, stabilizer, and antacid. Free from sewage sludge, it ensures the purity of food ingredients.

IFF Pharma SolutionsMETHOCEL™ K4M Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Functions:Controlled Release Agent, Suspending Agent, Binder, Thickener, Mucoadhesive, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
Dosage Form:Tablets
Labeling Claims:VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free
Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K4M Premium HPMC utilized in ceramics and pharmaceuticals, serves as a binder, film former, gelling agent, mucoadhesive, solubilizer, and suspension aid. It aids in granulation and exhibits water solubility.

METHOCEL™ K100M Premium HPMC - Specialty banner

IFF Pharma SolutionsMETHOCEL™ K100M Premium HPMC - Specialty

Functions:Green Strength Enhancer, Controlled Release Agent, Film Former, Anti-Settling Agent, Plasticizer, Rheology Modifier, Surfactant, Lubricant (Internal), Processing Aid, Thickener, Binder, Emulsifier
Chemical Name:Hydroxypropyl Methylcellulose
Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
End Uses:Ceramics
Dosage Form:Tablets
Certifications & Compliance:CFDA Compliant (China), Regulation (EC) No. 1333/2008, National Bioengineered Food Disclosure Standard, cGMP, GMP, Indian Pharmacopeia, Regulation (EU) No. 1829/2003, FDA 21 CFR 172.874, Hazard Analysis Critical Control Point (HACCP), IFANCA Halal, Swiss Ordinance (SR 817.023.21), Organic Certified, FEMA Compliant, Chinese Pharmacopeia (ChP), WEEE Directive 2012/19/EU, European Pharmacopeia (Ph. Eur.), USDA Organic, Kosher, FCC Compliant, FDA 21 CFR 182.1480, FFDCA, ICH Q3C, ISO 14001, Halal, FDA Compliant, Regulation (EU) No. 1169/2011, EU Packaging Directive (94/62/EC), Japan Pharmacopeia (JP), European Regulation 396/2005/EC, JECFA (FAO/WHO), EU Cosmetic Regulation 1223/2009 Compliant, British Pharmacopeia (BP), EXCiPACT, Doping-Free, 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, Directive 2023/915/EU, 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™ K100M Premium HPMC - Specialty is employed in ceramics as a binder, utilizing granulation in its manufacturing process. Within pharmaceuticals and nutraceuticals, it serves as a suspension aid, thickener, and viscosity modifier, boasting water solubility for versatile application.

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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