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6 Products found on IFF Pharma Solutions

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IFF Pharma SolutionsVitacel® VE - 650

Labeling Claims:Allergen-free, Vegetarian, Melamine-free, Vegan, BSE-free, Generally Recognized As Safe (GRAS), TSE-free, Phthalates-free, Not Listed In California Proposition 65, Nanomaterials-free
Certifications & Compliance:FDA 21 CFR Regulations, Nagoya Compliant, FDA Food Safety Modernization Act (FSMA)

Vitacel® VE - 650 boasts several labeling claims, including being BSE-free, Generally Recognized As Safe (GRAS), melamine-free, nanomaterials-free, not listed in California Proposition 65, phthalates-free, and TSE-free.

IFF Pharma SolutionsAquacoat® ECD - 30

Chemical Name:Ethylcellulose
Dosage Form:Tablets
Labeling Claims:Kosher, Paraben-free, Perfluorooctanoic Acid-free, Latex-free, Aluminum-free, PVC-free, Generally Recognized As Safe (GRAS), Nanomaterials-free, Caffeine Free, Heavy Metal-free, Hormones-free, APE-free, Natural Latex Rubber-Free, Halal, Ethylene Oxide-free, Vegan, Melamine-free, Glycerin-free, Endocrine Disruptor-free, TSE-free, Palm Oil-free, Dioxin-free, Monosodium Glutamate (MSG)-free, GMO-free, Dye Free, Colorants-free, Plasticizer-free, PHO (Partially Hydrogenated Oil)-Free, PFAS-Free, Antibiotics-free, Tributyl Tin Compounds-Free, Bisphenol A-free, Pesticide-free, Not Listed In California Proposition 65, Non-GMO, Vegetarian, Allergen-free, PFOS-free, Sugar-free, Genotoxic-free, Phthalates-free, BSE-free, Preservative-free, Triphenyl Tin Compounds-Free, PAH-free
Certifications & Compliance:European Pharmacopeia (Ph. Eur.), FCC Compliant, FDA Food Safety Modernization Act (FSMA), Doping-Free, European Regulation 396/2005/EC, Chinese Pharmacopeia (ChP), United States Pharmacopeia (USP), Regulation (EU) No. 231/2012, FDA Compliant, Nagoya Compliant, Japan Pharmacopeia (JP), cGMP, National Formulary (NF), GMP, British Pharmacopeia (BP), EXCiPACT, FDA 21 CFR Regulations

Aquacoat® ECD - 30 containing ethylcellulose, is a liquid formulation utilized for tablet coating. With labeling claims of being palm oil-free, glycerin-free, and endocrine disruptor-free, it serves as a controlled release agent, enteric coating system, sustained release agent, and taste masking agent in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsAccelerate® DS - 812

Chemical Name:Cellulose Gum, Croscarmellose Sodium
Dosage Form:Capsules, Granules, Tablets, Soft Chews, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Odor-free, Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Colorants-free, Nanomaterials-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, Nagoya Compliant, FDA 21 CFR Regulations
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 SolutionsAc-Di-Sol® SD - 711

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Capsules, Granules, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Nanomaterials-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:Halal, British Pharmacopeia (BP), China DMF, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, GMP, Nagoya Compliant, National Formulary (NF), FDA 21 CFR Regulations, Japan Pharmacopeia (JP)
Manufacturing Technology:Wet Granulation

Ac-Di-Sol® SD - 711 a powdered form of croscarmellose sodium, is utilized as a disintegrant and immediate release agent in pharmaceuticals and nutraceuticals. Its versatility is evident in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs), manufactured through wet granulation techniques.

IFF Pharma SolutionsAccelerate® DS - 813

Chemical Name:Cellulose Gum
Functions:Disintegrant
Manufacturing Technology:Wet Granulation
Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Vegan, Dye Free, Pesticide-free, GMO-free, Allergen-free, Aluminum-free, Generally Recognized As Safe (GRAS), Natural Latex Rubber-Free, PFAS-Free, Preservative-free, PFOS-free, Nanomaterials-free, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Not Listed In California Proposition 65, Palm Oil-free, Hormones-free, Melamine-free, Endocrine Disruptor-free, Sugar-free, Tributyl Tin Compounds-Free, Antibiotics-free, Glycerin-free, BSE-free, PVC-free, PAH-free, Phthalates-free, Triphenyl Tin Compounds-Free, Caffeine Free, TSE-free, Plasticizer-free, APE-free, Ethylene Oxide-free, Non-GMO, Vegetarian
Certifications & Compliance:Regulation (EU) No. 231/2012, ICH Q3C, European Pharmacopeia (Ph. Eur.), Nagoya Compliant, FDA 21 CFR Regulations, FDA Food Safety Modernization Act (FSMA), United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, cGMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), European Regulation 396/2005/EC, Doping-Free

Accelerate® DS - 813 is available in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs). Manufactured using wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical formulations. It is supplied in powder form for ease of processing and formulation.

IFF Pharma SolutionsAc-Di-Sol® SDW - 802

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Capsules, Granules, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Odor-free, Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Nanomaterials-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:Halal, British Pharmacopeia (BP), China DMF, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, Nagoya Compliant, National Formulary (NF), FDA 21 CFR Regulations, Japan Pharmacopeia (JP)
Manufacturing Technology:Wet Granulation

Ac-Di-Sol® SDW - 802 is a versatile ingredient suitable for capsules, granules, and orally disintegrating tablets (ODTs). Employing wet granulation, it serves as a disintegrant and immediate release agent in pharmaceutical and nutraceutical formulations.