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GAS Notice (GRN) No. 920
https://www.fda.gov/food/generallyrecognizedsafegras/grasnoticeinventory
Form Approved: OMB No. 09100342; Expiration Date: 02/29/2016
(See last page for OMB Statement)FDA
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How to fill out gras notice 920 thaumatin
How to fill out gras notice 920 thaumatin
01
To fill out GRAS notice 920 for thaumatin, follow these steps:
02
Begin by providing the contact information of the notifier, including the name, address, and email.
03
Specify the purpose of the notice and provide a detailed description of the intended use of thaumatin.
04
Include information about the substance itself, such as its chemical composition and manufacturing process.
05
Describe the history of use and consumption of thaumatin, including any relevant studies or research.
Who needs gras notice 920 thaumatin?
01
GRAS notice 920 for thaumatin is required by those who intend to use or market thaumatin as a food ingredient or additive.
02
This notice is typically submitted by food manufacturers, suppliers, and distributors.
03
It is essential for ensuring the safety and compliance of thaumatin with FDA regulations.
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What is gras notice 920 thaumatin?
GRAS Notice 920 pertains to thaumatin, a natural sweetener derived from the katemfe fruit. It is recognized as Generally Recognized As Safe (GRAS) for use in food products.
Who is required to file gras notice 920 thaumatin?
Manufacturers or food producers intending to use thaumatin as an ingredient in food products must file GRAS Notice 920.
How to fill out gras notice 920 thaumatin?
To fill out GRAS Notice 920, applicants must provide detailed information about the substance, its proposed uses, safety assessments, and any relevant scientific data supporting its GRAS status.
What is the purpose of gras notice 920 thaumatin?
The purpose of GRAS Notice 920 is to inform the FDA about the safety and intended use of thaumatin as a food ingredient, allowing for regulatory clarity and consumer protection.
What information must be reported on gras notice 920 thaumatin?
GRAS Notice 920 must report information such as the identity of the substance, data on its safety, conditions of use, intended consumer population, and any studies conducted on its effects.
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