Back to pharma.iff.com
All Categories
All Categories
Products
302
Brands
34
Documents
4226
Technologies
Segments
Markets
Products
IFF Pharma Solutions
All IFF Pharma Solutions
Search products
Matching Products
Categories
(1)
Show All 1 Categories
Pharmaceuticals & Nutraceuticals
Pharmaceuticals & Nutraceuticals
Markets
Labeling Claims
Certifications & Compliance
Physical Form
All Filters
6 Products
found on IFF Pharma Solutions
Most Viewed
SDS
With SDS
TDS
With TDS
IFF Pharma Solutions
Ac-Di-Sol® SDW - 802
Chemical Name:
Croscarmellose Sodium
CAS Number:
74811-65-7
Dosage Form:
Orally Disintegrating Tablets (ODTs), Granules, Capsules
Labeling Claims:
Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, 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, Artificial Flavor-Free, PAH-free, Odor-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, USP 232 Elemental Impurities Free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR Regulations, FCC Compliant, British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, FSSC 22000, Orthodox Union Kosher, China DMF
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.
IFF Pharma Solutions
Accelerate® DS - 813
Chemical Name:
Cellulose Gum
Functions:
Disintegrant
Manufacturing Technology:
Wet Granulation
Labeling Claims:
Dye Free, Plasticizer-free, Nanomaterials-free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Ethylene Oxide-free, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Antibiotics-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Not Tested on Animals, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, PVC-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Melamine-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free
Certifications & Compliance:
cGMP, Japan Pharmacopeia (JP), European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, Doping-Free, European Pharmacopeia (Ph. Eur.), Nagoya Compliant, United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EU) No. 1272/2008, IFANCA Halal, Generally Recognized As Safe (GRAS), FDA 21 CFR Regulations
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 Solutions
Vitacel® VE - 650
Labeling Claims:
Melamine-free, Vegan, Phthalates-free, Allergen-free, Generally Recognized As Safe (GRAS), Not Listed In California Proposition 65, Halal, Vegetarian, TSE-free, BSE-free, Nanomaterials-free
Certifications & Compliance:
Nagoya Compliant, FDA Food Safety Modernization Act (FSMA), IFANCA Halal, FDA 21 CFR Regulations
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 Solutions
Aquacoat® ECD - 30
Chemical Name:
Ethylcellulose
Dosage Form:
Tablets
Labeling Claims:
Paraben-free, Phthalates-free, Tributyl Tin Compounds-Free, Ethylene Oxide-free, Triphenyl Tin Compounds-Free, Non-GMO, Not Listed In California Proposition 65, Dye Free, GMO-free, Endocrine Disruptor-free, Natural Latex Rubber-Free, PVC-free, Pesticide-free, Glycerin-free, Colorants-free, Not Tested on Animals, PHO (Partially Hydrogenated Oil)-Free, BSE-free, Aluminum-free, Melamine-free, PAH-free, TSE-free, Amine-free, Caffeine Free, Vegan, Monosodium Glutamate (MSG)-free, Genotoxic-free, Palm Oil-free, Dioxin-free, APE-free, Preservative-free, Kosher, Nanomaterials-free, Bisphenol A-free, Sugar-free, Hormones-free, PFAS-Free, Vegetarian, Perfluorooctanoic Acid-free, Nitrosamines-free, Antibiotics-free, Heavy Metal-free, Plasticizer-free, Allergen-free, Generally Recognized As Safe (GRAS), Halal, PFOS-free, Latex-free
Certifications & Compliance:
EXCiPACT, Regulation (EU) No. 231/2012, Chinese Pharmacopeia (ChP), European Regulation 396/2005/EC, FSSC 22000, cGMP, European Pharmacopeia (Ph. Eur.), GMP, FCC Compliant, Doping-Free, Japan Pharmacopeia (JP), United States Pharmacopeia (USP), British Pharmacopeia (BP), IFANCA Halal, FDA Food Safety Modernization Act (FSMA), National Formulary (NF), Nagoya Compliant, Orthodox Union Kosher, FDA Compliant, 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 Solutions
Ac-Di-Sol® SD - 711
Chemical Name:
Croscarmellose Sodium
CAS Number:
74811-65-7
Dosage Form:
Orally Disintegrating Tablets (ODTs), Granules, Capsules
Labeling Claims:
Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, 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, Artificial Flavor-Free, PAH-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, USP 232 Elemental Impurities Free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
Certifications & Compliance:
Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR Regulations, FCC Compliant, British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, FSSC 22000, Orthodox Union Kosher, Regulation (EU) No. 1169/2011, IFANCA Halal, China DMF
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 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.
