Sep 30, 2026Market & Brand Development

Exporting Skincare to Saudi Arabia: The SFDA Document Checklist for Importers of Chinese-Manufactured Brands

The 8-item SFDA document pack for importing Chinese-manufactured skincare into Saudi Arabia: eCosma notification, GMP certificate, FSC, COA, ingredient list, CoC and GSO 1943 Arabic labels.

SFDA document checklist for exporting skincare to Saudi Arabia
Importing a Chinese-manufactured skincare line into Saudi Arabia is straightforward — if the document pack is complete. The Saudi Food and Drug Authority (SFDA) requires every imported cosmetic to be notified in its eCosma system before it can be traded, and the notification file is only as strong as the documents behind it. Most launch delays we see in the GCC trace back to the same root cause: the brand and the factory assumed somebody else was preparing the paperwork. Here is the full checklist — what each document is, who provides it, and where launches typically get stuck.

The Document Pack: Eight Items

• eCosma notification number — filed by your licensed Saudi importer through the GHAD system; without it, no product can be imported or traded.
• Saudi Commercial Registration listing cosmetics trading, plus the importer's GHAD account — confirmed during supplier onboarding.
• GMP certificate from the manufacturing site (ISO 22716 / GMPC) — registered with the notification as proof of production compliance.
• Free Sale Certificate or equivalent market authorization from the country of origin.
• Certificate of Analysis (COA) for the product — batch-level testing documentation.
• Full ingredient list with concentrations — used to verify restricted substances against the GSO Annexes.
• Certificate of Conformity (CoC) issued before shipment by an SFDA-approved body — required at customs clearance.
• Bilingual Arabic/English labels compliant with GSO 1943 — artwork approved before printing.

Who Provides What: Brand, Factory, Importer

The factory — your OEM/ODM partner — provides the production-side documents: GMP certificate, product formulation and composition details, COAs, and label files. The importer files the notification and holds the SFDA relationship. The brand coordinates — and should collect the complete pack into a single file before production starts, because every one of these documents references the others.

Where Launches Typically Get Stuck

The Free Sale Certificate gap

Some markets accept a declaration; Saudi Arabia's reviewers expect proper market-authorization evidence for the manufacturing site. Confirm the exact format your importer's consultant requires before production, not after.

Ingredient concentrations

The ingredient list filed with the notification needs concentrations to verify restricted substances. If your factory's formula sheet omits percentages, the file bounces. Ask for a notification-ready formula sheet as a deliverable of the development stage.

Arabic label artwork

GSO 1943 requires Arabic labeling alongside other languages. Artwork approved without an Arabic compliance review is artwork that gets reprinted.

How Your Factory Should Support the File

For OEM and ODM brands, the practical question is simple: can your factory confirm, in writing and against the updated requirements, that your formulas and documents remain compliant — and how fast can they rework any affected SKU? An experienced partner assembles the production-side document pack as a standard deliverable: GMP certificates, COAs, composition data, and label files that already respect GSO 1943. Our compliance and testing services cover this coordination from brief to bulk, and our dedicated overview of skincare product development for Saudi Arabia covers market and channel definition for the Gulf. The full SFDA notification requirements are broken down in our guide to exporting skincare to Saudi Arabia and the GCC. If you are assembling an import file for the Kingdom, contact our team — we will map the document pack to your product line before production locks.

Frequently Asked Questions

Who submits the eCosma notification — the brand or the importer?

A licensed Saudi entity: the importer or distributor with a Commercial Registration listing cosmetics trading and an active GHAD account. Foreign brands work through this local partner or an authorized representative.

Is a Certificate of Conformity the same as the notification?

No. The notification registers the product in the SFDA database; the CoC is issued per shipment by an approved body for customs clearance. Both are required.

Does the GMP certificate need to be from Saudi Arabia?

No — the GMP certificate is from the manufacturing country (for example, a Chinese factory's ISO 22716 or GMPC certificate). It is registered as part of the notification file to prove production-site compliance.

What should I ask my factory for first?

The notification-ready formula sheet and the GMP certificate — these two unlock the importer's filing. Everything else (COAs, label files, declarations) builds on them.

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