Knowde Enhanced TDS
Identification & Functionality
- Chemical Family
- Chemical Name
- Ingredient Origin
- Pharma & Nutraceuticals Functions
- Technologies
Features & Benefits
Applications & Uses
- Applications
- Application / Functionality
Zerose™ erythritol standard granular pharma excipient is recommended for use in nutraceutical and medicinal candies, lozenges, coatings and other confectionary items, in medicinal capsules, powders, liquids, and toothpaste, and in topical applications and ointments.
After milling, combined with a binder, this product can also be used in many different tablet forms. This produce improves sensorial acceptance of oral products by masking the off taste of certain actives. It provides good storage stability like mannitol because of its low hygroscopicity, unlike mannitol it is well tolerated and does not reduce gastro-intestinal transition time and
therefore allows optimal absorption of the actives used. It can also act as an osmolyte in topical applications.
Properties
- Nutritional Information
Value | Units | Test Method / Conditions | |
Added Sugars | 0 | g/100g | — |
Ash Content | 0 | g/100g | — |
Calcium Content | 0 | mg/100g | — |
Calories | 0 | kcal/100g | — |
Cholesterol | 0 | mg/100g | — |
Dietary Fiber | 0 | g/100g | — |
Iron Content | 0 | mg/100g | — |
Moisture Content | 0.04 | g/100g | — |
Potassium Content | 0 | mg/100g | — |
Protein Content | 0 | g/100g | — |
Saturated Fat | 0 | g/100g | — |
Sodium Content | 0 | mg/100g | — |
Sugar Alcohols | 99.96 | g/100g | — |
Total Carbohydrates | 99.96 | g/100g | — |
Total Fat | 0 | g/100g | — |
Total Sugars | 0 | g/100g | — |
Trans Fat | 0 | g/100g | — |
Vitamin D | 0 | mcg/100g | — |
Regulatory & Compliance
- Certifications & Compliance
- Grade
- Allergen Status
In accordance with the 2004 USA Food Allergen Labeling and Consumer Protection Act (FALCPA), no allergen declarations are required for this product.
- Applicable Certifications
- Certified Kosher by the Orthodox Union (OU)
- Certified Halal by the Islamic Food and Nutrition Council of America (IFANCA)
- Regulatory Status
Zerose™ erythritol standard granular pharma excipient is produced in accordance with current food Good Manufacturing Practices (GMPs) under a comprehensive Hazard Analysis and Critical Control Points (HACCP) program and in compliance with applicable parts of 21 CFR, part 117 of the Code of Federal Regulations.
Zerose™ erythritol standard granular pharma excipient is produced in accordance with IPEC-PQG Good Manufacturing Practices.
Zerose™ erythritol standard granular pharma excipient complies with the United States Pharmacopeia (USP 39/NF34) monograph for erythritol, the Food Chemicals Codex 9th edition (FCC IX) monograph for erythritol, the JPE (1998) monograph for erythritol, and the European Pharmacopeia (8.0) monograph for erythritol.E-Number (E-NR): E968
Packaging & Availability
- Packaging Type
- Packaging
20 kg. paper bags with inside PE lining and super sacks
Material Numbers:
110004342 - 20 kg. bag
Storage & Handling
- Shelf Life
- 3 years
- Storage / Shelf-life
Product should be stored in a clean, dry, and odor-free area at ambient temperature and humidity.
The recommended best before date for Zerose™ erythritol standard granular pharma excipient under these conditions and in original unopened packaging is 3 years from the date of manufacture. For product in super sacks, the recommended best before date is 2 years from the date of manufacture. Product stored beyond the best before date should be evaluated
periodically for fitness of use.