Can you produce sunscreen lotion that meets U.S. broad spectrum requirements without greasy feel?

Yes-we can develop a lightweight, non-greasy sunscreen lotion and support U.S. broad spectrum claim substantiation with testing and documentation. Final labeling/claims should be confirmed with your U.S. regulatory advisor; we can assist with required test coordination.

US buyer view Launch planning Updated: January 27, 2026
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Best for
US brand owners, Amazon/FBA sellers, distributors, and private label buyers
Core intent
Who submits, what data is needed, and how to plan timelines before production

Quick Answer (for busy buyers)

Here’s the buyer-first summary. If your brand name is on the label, you usually act as the responsible person and must ensure the listing is submitted and kept current.

  • Yes.
  • At LAEYO Labs (Guangzhou), we can build a sunscreen lotion texture focused on fast-absorbing, non-greasy slip (e.g., lighter emulsions and film-former balance) while formulating toward U.S. broad spectrum positioning.
  • You will approve the concept, formula direction, and final lab sample before scale-up.
  • For compliance support, we can coordinate testing and documentation rather than “guarantee approval.” Our R&D setup includes dedicated labs (including efficacy testing and microbial challenge capability), and we can help arrange SPF/broad spectrum-related substantiation, stability, and microbiology documentation packages needed for your brand files and Amazon listing claims.
  • Operationally, we support OEM/ODM from formula customization and sampling through packaging and delivery.
  • MOQ is quoted case-by-case and is often driven by packaging factory minimums (tube/bottle/carton).
  • Typical timelines: one-stop brand landing about 45-60 days; bulk production about 10-20 working days after final sample.
  • Packaging ordering usually needs 10-30 working days (e.g., tube 15 days, glass bottle 15 days, acrylic bottle 30 days; single carton 15 days, set box 20 days).
Buyer outcome
A launch-ready compliance plan: inputs collected, roles assigned, and update cadence defined.
Most common blocker
Missing facility information + inconsistent ingredient/label snapshots across SKUs.
⚠️
This page is a practical buyer guide. For definitive requirements and updates, use FDA resources and qualified regulatory counsel.
  • Our team will answer your inquiries within 8 hours.
  • Your information will be kept strictly confidential.

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Thanks — we’ve received your request. Our team will follow up shortly. we typically reply within 8 hours (often sooner).