UNI-PURE® F

Native Starch, Corn

USP-NF, Ph. Eur., JPE

Description

Multi-compendial Native Starch can be used as a Filler and binder

Key benefits

  • NMT 15% Moisture
  • Inhibits the caking of hygroscopic materials
  • Can be used as a binder in Wet Granulation (when cooked)
  • EIP Index available

Functionalities

  • Filler
  • Diluent
  • Bulking agent
  • Binder
  • Disintegrant

Dosage form

  • Tablets Tablets
  • Hard Capsules Hard Capsules
EIP Documentation updated in Dec. 24

Product documentation

This product has 26 documents

Document nameDescriptionDownload
UNI-PURE® F EIP Index

Shows all documentation available on EIP (Excipient Information Package), which ones are public and on demand

UNI-PURE® F Specimen CoA

Certifies the quality of the excipient and demonstrates the batch meets the defined specification

UNI-PURE® F Release Specification

Shows the quality standards of a material according to a list of tests required

UNI-PURE® F MSDS

MSDS: Material Safety Data Sheet

UNI-PURE® F Label

Displays the label graphic

UNI-PURE® F TSE BSE

TSE (Transmissible Spongiform Encephalopathy) and BSE (Bovine Spongiform Encephalopathy)

UNI-PURE® F Source of origin

The country of origin of the excipient

UNI-PURE® F Regulatory Compliance

Compendial compliance (for example, USP-NF, Ph. Eur or BP, JP, JPE) and other regulatory status

UNI-PURE® F Non-GMO

A declaration that the material is not derived from a Genetically Modified Organism (GMO)

UNI-PURE® F Heavy metal

Reports the detection and estimation of the Heavy Metals

UNI-PURE® F Elemental impurities

Shows the evaluation for elemental impurities and if the excipient complies with the limits specified in ICH Q3D

UNI-PURE® F Nitrosamine

A risk assessment to ensure that there is no contamination of Nitrosamine and related compounds in the material

UNI-PURE® F Allergen

Related to Regulation or specific allergens evaluated

UNI-PURE® F Gluten free

The statement “Gluten-free” applies only if the gluten content in the medicinal product is less than 20 parts per million (ppm)

UNI-PURE® F Microanalytical

Report which shows Microbial limit test results

UNI-PURE® F Residual solvent

Declares that the levels of residual solvents in the material meets the limits defined by the pharmacopeia

UNI-PURE® F GRAS

GRAS: Generally Recognized as Safe

UNI-PURE® F Storage condition

The acceptable variations in temperature and relative humidity of storage facilities for formal stability studies

UNI-PURE® F Latex free

Certifies that the material is not made with natural rubber latex, latex derivatives

UNI-PURE® F Genotoxic free

Declaration if the material is free from Genotoxic Impurities

UNI-PURE® F Country of origin

It is the country of manufacture or production

UNI-PURE® F Aflatoxins

Declaration that the material is free from Aflatoxins

UNI-PURE® F Melamine

Declaration that confirm if the material is free of melamine contamination

UNI-PURE® F Shelf life

The duration, normally expressed in months or years from the date of manufacture, throughout which the excipient should continue to conform to the specification.

UNI-PURE® F Halal

Halal indicates that this product is permitted and fit for consumption according to Islamic law

UNI-PURE® F Kosher

Certifies that this ingredient and the process of preparing it complies with orthodox kosher