Call(WhatsApp Us)
+8618988990383Email Us
postmaster@laeyolabs.com广州市花都区花山镇华辉路18号
微观化妆品创意产业园E栋整栋Bringing a new sunscreen from idea to first purchase order (PO) in 2026 requires more than just a strong formula—it demands regulatory alignment, packaging readiness, and timeline discipline. This guide walks brand owners and…
Bringing a new sunscreen from idea to first purchase order (PO) in 2026 requires more than just a strong formula—it demands regulatory alignment, packaging readiness, and timeline discipline. This guide walks brand owners and sourcing managers through every actionable stage, from sampling to batch release, to keep your launch compliant and on schedule.
Before requesting samples, confirm whether your sunscreen qualifies as a cosmetic, OTC drug, or therapeutic good—this determines testing and labeling requirements.
Once specifications are defined, initiate lab sampling with your manufacturer’s R&D team.
Document package testing alongside formula refinement—UV filters and emulsifiers often react with plastics and coatings. Compatibility failures are one of the most common sources of project delays.
Once your formula is finalized, start efficacy and safety validation while packaging production proceeds in parallel.
| Test Item | Purpose | Turnaround | Evidence to Request |
|---|---|---|---|
| SPF/UVA in vivo or ISO 24444/24443 | Regulatory efficacy proof | 3–4 weeks | Final report signed by accredited lab |
| Preservative efficacy (Challenge Test) | Microbial safety | 2 weeks | Micro test report (ISO 11930) |
| Stability & Compatibility | Shelf life and packaging validation | Ongoing (up to 12 weeks) | Accelerated stability summary |
Once both the formula and test results meet specs, lock the packaging spec and design.
Before placing your first PO, ensure all compliance files are complete.
Depending on region and capacity, full projects take 40–75 days from first sample to finished goods:
Initial approval typically takes 1–2 weeks for existing base formulas or 3–4 rounds for full customization (30–40 days total).
Yes, but require them to provide packaging safety data and compatibility results. Always submit packaging samples for lab compatibility testing with the formulation.
Most OEMs offer 1000–3000 unit MOQs, depending on packaging and formula complexity. Small batches for sampling may be negotiated.
After locking your formula and primary packaging info—some markets require test reports and INCI lists upfront for portal submissions.
If rebranding an existing proven base, yes. Use existing 12-month stability data with matching packaging; otherwise, at least 3-month accelerated data is required before first shipment.