Food Supplement Registration in Saudi Arabia

Food supplements containing vitamins and minerals should be labeled in accordance with the General Guidelines on Claims (CAC/GL 1-1979) and the Codex Standard for the Labelling of Prepackaged Foods (Codex-Stan 1-1985, Rev. 1- 1991).

The product will be branded as a “food supplement” and will list the specific nutrient category(ies) or vitamin(s) and/or mineral(s) that it contains, depending on the situation.

The product’s label should list the vitamins and minerals that are included in it in numerical form. Weight units that comply with the Codex Guidelines on Nutrition Labelling (CAC/GL 2-1985 Rev.1-1993) should be used.

The indicated vitamin and mineral contents should correspond to the portions of the product that are advised for daily consumption; if this is not the case, the amounts per unit for a single usage may also be provided.

Additionally, vitamin and mineral information must be expressed as a percentage of the nutrient reference values listed in the Codex Guidelines on Nutrition Labelling, if applicable.

The product’s label should specify how it should be used (amount, frequency, and any unique circumstances).

The consumer is advised not to exceed the maximum amount in one day by the label.

Frequently Asked Questions: Food Supplement Registration in Saudi Arabia

1. What is the process for registering a food supplement in Saudi Arabia?

Food supplement registration in Saudi Arabia involves submitting an application to the Saudi Food and Drug Authority (SFDA). The process includes providing product details, ingredients, labeling, and manufacturing information for evaluation.

2. How long does it take to register a food supplement with the SFDA?

The registration process typically takes 2-6 months, depending on the completeness of the application and the complexity of the product. Ensuring all documents meet SFDA requirements can help avoid delays.

3. What documents are required for food supplement registration in Saudi Arabia?

Required documents include product composition, Certificate of Analysis (COA), Good Manufacturing Practice (GMP) certificate, product labeling in Arabic and English, and proof of safety and efficacy.

4. Are there specific labeling requirements for food supplements in Saudi Arabia?

Yes, the SFDA requires labels to include product name, ingredients, usage instructions, warnings, storage conditions, and expiry date. Labels must also be translated into Arabic.

5. Do I need a local representative to register a food supplement in Saudi Arabia?

Yes, foreign manufacturers are required to appoint a Saudi Authorized Representative (SAR) to handle the registration process and ensure compliance with SFDA regulations.