Product development
Halal-focused sheet-mask OEM.
Develop a single-use sheet mask with serum around your brand, packaging and destination. Halal documentation is reviewed for the actual product, ingredients, site and proposed brand.
Named products you can check in the Halal record.
The BPJPH record includes the following sheet mask product names. Use the actual annex and formula identity to establish whether an existing record is relevant to your project. A new brand or altered product still needs a scope review.
- Dr.Leo Niacinamide 377 VC Brightening Facial Mask
- Dr.Leo 7X Ceramide Repair & Soothing Facial Mask
A practical starting specification.
| Decision | Reference or project input |
|---|---|
| Product format | Single-use sheet mask with serum |
| Packaging reference | Define the sheet material, serum loading, pouch, seal and outer packing in the sample specification. |
| Formula direction | The registry includes named niacinamide and ceramide facial-mask products. New sheet materials, serum formulas and brand identities are reviewed for the actual project. |
| MOQ and commercial terms | Confirmed for the selected formula, packaging components and order quantity |
| Samples and schedule | Scope, charges, freight, tests and approval milestones are agreed in the quotation |
What to send for a useful proposal.
- Sheet material and fit preferences
- Serum texture, intended routine and ingredient direction
- Serum loading, pouch design and carton requirements
- Quantity, destination, sample and document needs
Review the sample and packaging together.
Review sheet/serum compatibility, pouch sealing, stability, microbiological requirements and application instructions.
A reference pack is a starting point for development, not a current stock or price offer. Confirm the final material, net content, decoration and quantity before production.
Connect the formula to the certificate scope.
The official registry includes named products, not every possible private-label formula. Confirm whether your project matches an existing product record or requires a further review. Changes in formula, raw-material sourcing, product identity or site can change the documentation work.
Plan production and handover.
Agree on the approved formula and pack, artwork, relevant tests, material readiness and production window. Confirm batch identification, inspection records, shipping responsibilities and the destination documentation in your order.
Manufacturer documentation reviewed: 4 November 2026.