What is Feverfew Extract 20:1?
Feverfew Extract 20:1 is a standardized herbal extract (20:1). It is used as a raw material in dietary supplement production.
Product Features
- Part Used: Above Ground
- Standardization: 20:1
- Solubility: Water-soluble
| Analysis | Value |
|---|---|
| Moisture | ≤5.0 % |
| Total Heavy Metals | ≤10 ppm |
| E. Coli | Negative in 10 g |
| Salmonella | Negative in 25 g |
What is it Used For?
Feverfew Extract 20:1 is used in dietary supplements to support headache/migraine comfort. With its standardized 20:1 content, it provides a consistent source of botanical ingredients in tablet, capsule, and powder formulations.
Main areas of use: Herbal Products, Capsule Filling, Tablet Manufacturing.
- Natural Source: Preserves its natural content through the extract of the Tanacetum parthenium plant.
- Production Compatibility: Its powder structure is suitable for tablet and capsule production processes.
- Technical Documentation: COA, SDS, TDS, and other requested technical documents are provided in full.
Forms of Use (Tablet, Capsule, Powder)
The powder form can be used in tablet, capsule, powder mix/sachet, and (due to water solubility) liquid/syrup formulations.
Positive Plant List Check
Feverfew Extract 20:1 is included among the permitted (positive) plants under the Turkish Food Codex dietary supplement legislation. The permitted/used part is: Above Ground.
Usage Rate in Dietary Supplements
According to the Restricted Substances List for Dietary Supplements, a daily usage limit of 500mg/day applies to this component/extract.
Storage, Shelf Life, and Re-test
Store in a cool, dry, and protected from light environment. The recommended re-test period is generally 3 years; it may vary by manufacturer. The CoA document of the relevant batch shall be taken as the basis for the exact date.
Technical Documents and Supply — Asuka Kimya
You can contact Asuka Kimya for SDS, TDS, CoA, and supply conditions for Feverfew Extract 20:1.