Label Compliance Review

Submit your label artwork. We audit every panel against NMRA Act No. 27 of 1980 and SLS 1587:2018, run an independent Gemini peer review, and verify findings with the RAQ Consultation Regulatory Team — branded PDF delivered within 24 hours of payment verification.

NMRA & SLS 1587:2018 labelling rules: mandatory disclosures (INCI list, manufacturer, batch, PAO, net content, category warnings, importer, trilingual text) must be legible on the artwork as printed. We check every panel you give us — for one product (one SKU). One SKU per order
1

About you

2

About the product

3

Label information (declared)

Type these exactly as they appear on your artwork. We use these declarations to verify presence on the artwork rather than re-reading small text — which is more reliable than asking AI to transcribe small print. If a field is not present on your artwork (e.g., no batch number printed), tick the "not present" option where available.

Type the manufacturer name verbatim as printed on the label.
Verbatim, including city/country.
The Sri Lankan importer or marketer.
Verbatim, including city.
Type the batch format you print, OR "varies per batch", OR "not present" if no batch field on artwork.
Choose the format used on your artwork.
Choose the format used on your artwork.
4

Upload artwork — your way

How does your label come? Pick the layout that matches your artwork. We'll review whatever you give us.
Accepted formats: PDF, JPG, PNG, WEBP. Minimum resolution: 2400×3000 pixels per panel for image uploads. PDFs are automatically converted to high-resolution images before review. Most modern design software exports meet this — if your file is rejected, re-export at higher resolution from your source file.

5

What are you submitting?

Pre-production artwork review treats placeholder fields (like XXXXXX or MM/YYYY) as structural compliance. Finished product review requires populated values. If unsure, select strict review.

Your artwork stays private. Used only for this review.

Reports are advisory; final regulatory authorisation rests with NMRA. RAQ Consultation Regulatory Team verifies report findings before release but cannot guarantee NMRA acceptance.