In one line: European manufacturer, products made in the EU; white label from more than 500 ready-made formulas, private label from your own; Certificate of Analysis and specification with every batch; ISO 22000, GMP and HACCP certified, registered with the US FDA as a food facility; the group behind HYPERPHARM ships to more than 40 countries, and Saudi Arabia is one of its main markets; reply within 24 hours, Monday to Friday.
In Saudi Arabia a company in the country, such as your importer, files the registration with the Saudi Food and Drug Authority (SFDA). We supply the manufacturer's side of the file: the Certificate of Analysis and specification of each batch, copies of the plant's certificates, the Certificate of Free Sale and the Certificate of Manufacture, and the apostille or consular legalisation where the file asks for it. The carton is laid out in Arabic, to the label rules your importer confirms.
| Question | Saudi Arabia | Source |
|---|---|---|
| Regulator | Saudi Food and Drug Authority (SFDA). Supplements go through the food sector, or through the drug sector as herbal and health products | SFDA Food Sector pre-registration guide, file of July 2024; SFDA Top Deficiencies in Herbal and Health Products, v1.1 |
| Who files | A company in Saudi Arabia, such as your importer, with the manufacturer's documents | SFDA conditions for food clearance, file of April 2025 |
| Label language | Arabic; another language may stand alongside it, identical in content | SFDA FAQ on food labels (SFDA.FD/GSO 9), updated 18 July 2024 |
| Dates on the pack | Production and expiry dates engraved, embossed or stamped on the pack or its original label; date stickers are not permissible | USDA FAIRS Saudi Arabia, SA2023-0004, 26 July 2023 |
| Papers from the manufacturer | Free sale certificate; stability study for the proposed shelf life (up to five years); leaflet for tablets, capsules and pills; a Pharmaceutical GMP certificate "or equivalent" for pills, tablets and capsules | SFDA Food Sector pre-registration guide, July 2024 |
| Halal | A halal certificate for food products that require one, and proof behind any halal logo | SFDA conditions for food clearance, April 2025 |
| Apostille | Saudi Arabia is a party to the Apostille Convention, in force since 7 December 2022 | HCCH status table, update of 30 June 2026 |
| WHO long-term condition | 30 °C/65% RH, which corresponds to zone IVa | WHO stability list, March 2021 |
| Customs | Declaration on Fasah no later than 48 hours before arrival; the importer registers on Ghad | US International Trade Administration, Saudi Arabia country guide, May 2026; SFDA food clearance conditions |
Can I get private label or white label supplements made for Saudi Arabia?
Yes. White label uses one of more than 500 ready-made formulas, with new ones added every month; private label is made to your own formula, and if you bring your own formula, it stays yours. Both go into stock packaging (bottles, tubes, pouches, sachets) or into a blister with a printed carton.
The plant lays out and prints the label and the carton in Arabic, or prints from your own artwork. A sample goes out before an order, a visit to the plant is possible, and delivery is worldwide, EXW by default, FCA or DAP on request. Standard shelf life is 24 months. The manufacturing group behind HYPERPHARM ships to more than 40 countries, and Saudi Arabia is one of its main markets, with the United Arab Emirates and Lebanon. See the UAE, Saudi Arabia and Lebanon for the wider Gulf view.
What is the minimum order for supplements for a Saudi importer?
The smallest start is a ready-made formula in stock packaging: from 100 units, with production from 2 weeks. The figures rise from there, in the order of the table below.
| Your start | Minimum | Production |
|---|---|---|
| Ready-made formula, stock packaging | From 100 units | From 2 weeks |
| Your own formula, bottles | From 500 bottles | From 4 weeks |
| Tablets or capsules in blisters, carton printed for your brand | From 2,000 cartons and at least 4,000 blisters, with a ready-made formula or your own | From 2 weeks |
A repeat order has the same minimum as the first. Each blister carton holds 1 to 4 blisters, one kind of tablet or capsule per blister, and the lidding foil is printed with your brand. Full figures by format are on the minimum order page and the lead times page. Tablets and capsules are sealed on an Uhlmann B 1240 and cartoned on an IMA IC 150; see tablets in blisters and capsules in blisters.
Who registers a food supplement with the SFDA: the manufacturer or the importer?
A company in Saudi Arabia, such as your importer, files with the SFDA; the brand owner and the importer prepare the application, and the approval is the SFDA's decision. The manufacturer's part is the document set the file draws on, and that is where HYPERPHARM works for you.
Two things are settled before filing: the route and the dosage form. The SFDA takes supplements through its food sector or, as herbal and health products, through its drug sector, and your importer settles the route with the SFDA. For customs, the importer registers its establishment and products on the Ghad platform and declares each shipment on Fasah; the steps are in our article on the Saudi food clearance file.
What does the SFDA ask the supplement manufacturer for?
Papers that depend on the route and the dosage form. For the food route, the SFDA's pre-registration guide (file of July 2024) lists the items below; next to each is what we supply.
- A free sale certificate from the country of origin. We arrange the Certificate of Free Sale and the Certificate of Manufacture. See export documents.
- A stability study based on the shelf life you propose, which may not exceed five years. Our standard shelf life is 24 months. Send the shelf life and the pack you plan with your enquiry, and our reply confirms what supports it.
- For products sensitive to heat, humidity or sunlight, a document describing the packaging material and its safety. The blister films offered for your product are PVC, PVC/PVDC and cold-formed aluminium (alu-alu), with lidding foil of aluminium; the film is confirmed in our reply. See blister films.
- A leaflet for tablets, capsules and pills. A printed leaflet goes into the carton, to your artwork, in Arabic for Saudi Arabia.
- For pills, tablets and capsules, a Pharmaceutical GMP certificate "or equivalent". The plant is ISO 22000, GMP and HACCP certified by BM Certification, with GMP for food supplements audited against the Food Supplements Europe guide; copies of the certificates with their numbers go to you on request, and your importer confirms with the SFDA which certificate set it accepts for the file.
- A certificate of analysis and a specification. Both come with every batch.
Is my supplement a food or a medicine for the SFDA?
The SFDA decides it on contents and claims, and the pack does not change it. Its Products Classification Guidance (version 8.0, 20 November 2024) treats a supplement as a pharmaceutical product when it contains a medicinal herb, exceeds the daily limit of technical standard SFDA.FD 55, is intended to treat, prevent or diagnose a disease, contains an active pharmaceutical ingredient, or is not intended for ingestion. Blister is not on the list.
That makes the carton text part of the registration question: no disease statement on the carton, foil or website, doses within the limit and no medicinal herb unless you want the pharmaceutical route. The full set of triggers and eight published SFDA decisions are in food supplement or medicine in Saudi Arabia, and the general question is in does a blister make a supplement a medicine. Your importer or the brand owner can ask the SFDA to classify a product before print; we advise doing it before the first order.
A third-party accredited laboratory can test your product for prohibited substances on request, with the report in your brand's name.
Which language and which dates go on a supplement carton for Saudi Arabia?
Arabic, with any other language alongside it and identical in content. The SFDA's rule reads "Labelling and adjoining explanatory statements shall be in Arabic". The plant lays out the carton to the label rules your importer confirms, or prints your artwork; see Arabic and French packaging and the blister artwork guide.
Dates are printed, not stuck on. Under the food rules summarised by the US Department of Agriculture in July 2023, production and expiry dates are engraved, embossed or stamped on the pack or its original label, one pair only, and date stickers are not permissible. The batch number, the production date and the expiry date are printed on the carton, and the dates are never a sticker; your importer confirms the format.
Is halal certification needed for supplements in Saudi Arabia?
The SFDA asks for a halal certificate for food products that require one and for proof behind any halal logo. Halal certification is arranged for each batch of your product, when your market asks for it, so the certificate names the product that is on your carton.
There are two routes, and the choice is yours: a certification body visits and issues the certificate, or a halal auditor is present at the production of the batch. Raise it in your enquiry, before the carton is printed. More on halal supplements.
What documents does a supplement shipment need to clear Saudi customs?
The SFDA clearance text lists a commercial invoice with products, quantities, expiry dates and batch numbers, a certificate of origin, a bill of lading and, for dietary supplements, a marketing certificate from the country of origin. Proof behind a halal logo is added if the carton shows one. Your importer files; we supply the batch documents.
The invoice, the Certificate of Analysis and the carton carry the same batch number and expiry date, so the file agrees from the plant to the port. The SFDA may take samples from a consignment, at the importer's expense. Delivery is EXW by default, FCA or DAP on request; Saudi import clearance and duties stay with the buyer under all three. The full list is in the Saudi food clearance file.
Does Saudi Arabia accept an apostille?
Saudi Arabia has been a party to the Apostille Convention since 7 December 2022, so an apostille is available for the manufacturer's documents. Your importer confirms with the SFDA that the apostille is taken for your file. We arrange the apostille or the consular legalisation, whichever the file calls for.
Do blisters suit Saudi Arabia's heat?
WHO's list gives Saudi Arabia a long-term condition of 30 °C/65% RH, which corresponds to zone IVa; the SFDA food guide names no testing condition. In a blister each dose stays sealed in its own cavity until it is pushed out, and how much moisture reaches it depends on the film. PVC, PVC/PVDC and alu-alu are offered as options for your product, and the film is confirmed in our reply.
The list was written for medicines and serves as a reference for supplements. See blister packaging for hot and humid markets and climatic zones by country.
Why buy supplements for Saudi Arabia from HYPERPHARM?
You start from 100 units in stock packaging. Blisters start from 2,000 cartons, and the papers your importer needs arrive with the goods. The rows below show what you get and what your importer adds.
| Item | From us | From your importer |
|---|---|---|
| Minimum order | Ready-made formula in stock packaging from 100 units. Blisters from 2,000 cartons. Production from 2 weeks | Confirms the quantity for the first shipment |
| Application | Documents for the file | Settles the route with the SFDA and files |
| Carton and label | Laid out and printed in Arabic, with the lidding foil printed with your brand; your own artwork can be used instead | Confirms the label rules and any numbers |
| Dates | Batch number, production date and expiry date printed on the carton | Confirms the format the carton must show |
| Batch documents | Certificate of Analysis and specification with each batch; certificate copies on request | Adds them to the file |
| Certified documents | Certificate of Free Sale, Certificate of Manufacture, apostille and consular legalisation where the file asks for them | Confirms how the SFDA wants them certified |
| Halal | Arranged for each batch of your product, when your market asks for it | Confirms whether the product needs it |
What your product decides
Each line shows the cost in time, quantity or risk, not in money.
| Your product or plan | What changes | Trade-off |
|---|---|---|
| A first launch with a ready-made formula | Stock packaging, carton printed by the plant | Quantity and time: from 100 units, production from 2 weeks |
| Tablets or capsules in a blister | One kind per blister, each dose sealed until it is pushed out, carton in Arabic | Quantity and time: from 2,000 cartons and 4,000 blisters, production from 2 weeks |
| Tablets or capsules sensitive to heat, humidity or sunlight | The SFDA guide asks for a document on the packaging material | Time: the document is agreed before filing |
| A claim that refers to a disease, or a dose above the SFDA limit | The SFDA is likely to treat the product as a medicine | Risk: a different file and a carton printed for the wrong route |
| A halal logo on the carton | The SFDA asks for proof behind the logo | Time: a certificate for your batch, ready before shipping |
| Carton text changed after your importer's check | New artwork and a new print | Time and quantity: the carton and foil are reprinted |
Questions buyers ask about supplements for Saudi Arabia
Is there a European manufacturer of private label supplements for Saudi Arabia?
Yes. HYPERPHARM is a European manufacturer, made in the EU, with white label from more than 500 ready-made formulas and private label from your own formula. A ready-made formula in stock packaging starts from 100 units, with production from 2 weeks. Saudi Arabia is one of the main markets of the manufacturing group behind it.
What is the minimum order for private label supplements for Saudi Arabia?
From 100 units for a ready-made formula in stock packaging, with production from 2 weeks. Your own formula starts from 500 bottles, with production from 4 weeks. Tablets and capsules in blisters start from 2,000 cartons and at least 4,000 blisters, with production from 2 weeks.
Who registers a food supplement with the SFDA?
A company in Saudi Arabia, such as your importer, files with the SFDA, with the manufacturer's documents. We supply the Certificate of Analysis and specification of each batch, copies of the plant's certificates, the Certificate of Free Sale and the Certificate of Manufacture. The approval is the SFDA's decision.
What does the SFDA ask of the manufacturer of a supplement?
For the food route, the SFDA's pre-registration guide of July 2024 lists a free sale certificate, a stability study for the proposed shelf life, a leaflet for tablets and capsules, a document on the packaging material for heat-sensitive products and a Pharmaceutical GMP certificate "or equivalent" for pills, tablets and capsules. Your importer confirms the list for your product.
Which GMP certificate does the plant hold for an SFDA file?
The plant is ISO 22000, GMP and HACCP certified by BM Certification, with GMP for food supplements audited against the Food Supplements Europe guide, and registered with the US FDA as a food facility. Copies with their numbers go to you on request, and your importer confirms with the SFDA which certificate set it accepts.
When does the SFDA treat a food supplement as a medicine?
When it contains a medicinal herb, exceeds the daily limit of standard SFDA.FD 55, is intended to treat, prevent or diagnose a disease, contains an active pharmaceutical ingredient or is not meant for ingestion. A blister does not change the class. Details are in our article on the SFDA's classification triggers.
Must the supplement label for Saudi Arabia be in Arabic?
Yes. The SFDA rule says labelling and adjoining explanatory statements shall be in Arabic, and another language may stand alongside it, identical in content. The plant lays out and prints the carton to the label rules your importer confirms.
Can the expiry date be a sticker on a supplement carton for Saudi Arabia?
No. Under the food rules summarised by the US Department of Agriculture in July 2023, date stickers are not permissible. The production date, the expiry date and the batch number are printed on the carton.
Do I need a halal certificate for supplements sold in Saudi Arabia?
The SFDA asks for one for food products that require it and for proof behind any halal logo. Halal certification is arranged for each batch of your product, when your market asks for it, by a certification body or by an auditor present at production.
Does Saudi Arabia accept an apostille on export documents?
Saudi Arabia is a party to the Apostille Convention, in force since 7 December 2022. Your importer confirms with the SFDA that the apostille is taken for your file, and we arrange the apostille or the consular legalisation, whichever the file calls for.
What storage condition does WHO list for Saudi Arabia?
30 °C/65% RH, which corresponds to zone IVa. The list was written for medicines and serves as a reference for supplements; the SFDA food guide names no testing condition.
Read more
The UAE, Saudi Arabia and Lebanon · Saudi food clearance file for supplements · Food supplement or medicine in Saudi Arabia · Does a blister make a supplement a medicine · UAE supplement registration documents · Export documents · Halal supplements · Minimum order quantity · Lead times · Blister packing · Blister films · Blister artwork guide · Arabic and French packaging · Blister packaging for hot and humid markets · Climatic zones by country · Quality and batch documents · Supplement manufacturer for distributors · Blister or bottle
Ask about supplements for Saudi Arabia
Send us the product, the format, the quantity and the list your importer or the SFDA has given you. We answer within 24 hours, Monday to Friday.
Request a quote → Email sales@hyperpharm.eu
Sources
- Saudi Food and Drug Authority, Food Sector: Guide to Pre-registration Evaluation for Food Products (file of July 2024). Used for: free sale certificate, stability study and maximum shelf life of five years, document on packaging material, leaflet, GMP certificate "or equivalent". sfda.gov.sa. Checked 9 and 14 October 2026.
- Saudi Food and Drug Authority: Conditions and Requirements for Food Clearance (file uploaded April 2025). Used for: Fasah and Ghad, invoice content, marketing certificate, halal evidence, samples. sfda.gov.sa. Checked 14 October 2026.
- Saudi Food and Drug Authority: FAQ on the language of food labels (SFDA.FD/GSO 9), answer updated 18 July 2024. sfda.gov.sa. Checked 14 October 2026.
- Saudi Food and Drug Authority: Products Classification Guidance, version 8.0 (OPS-G-002), 20 November 2024, Note 3. sfda.gov.sa. Checked 14 October 2026.
- Saudi Food and Drug Authority: Top Deficiencies in Herbal and Health Products, version 1.1, 8 December 2020 (the drug sector's route). sfda.gov.sa. Checked 9 October 2026.
- US Department of Agriculture, Foreign Agricultural Service: Food and Agricultural Import Regulations and Standards, Country Report, Saudi Arabia, SA2023-0004, 26 July 2023. Written for food. Copy on agriexchange.apeda.gov.in. Checked 14 October 2026.
- US International Trade Administration: Saudi Arabia, Import Requirements and Documentation (Country Commercial Guide), last published 11 May 2026. trade.gov. Checked 14 October 2026.
- Hague Conference on Private International Law: status table of the Apostille Convention, last update 30 June 2026 (Saudi Arabia in force since 7 December 2022). hcch.net. Checked 13 October 2026.
- World Health Organization: Stability conditions for WHO Member States by Region, update of March 2021. Written for medicines. who.int. Checked 9 October 2026.
