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What stability test is recommended for eye cream (heat, freeze-thaw, shelf life) for U.S. sales?

For U.S. sales, we typically recommend a combined stability plan: accelerated heat, freeze-thaw cycling, and real-time shelf-life, plus packaging compatibility. We can support third-party testing, documentation, and batch records to back your label claims.

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.

  • For an eye cream sold in the U.S. (including Amazon), we usually propose a stability package that covers: accelerated heat (e.g., 40C with humidity where applicable), freeze-thaw cycling (multiple cycles to stress emulsions), and real-time shelf-life at ambient conditions.
  • We also include packaging compatibility (formula vs. tube/bottle/closure) to reduce risks like separation, discoloration, odor change, leakage, or viscosity drift.
  • We can support documentation and testing coordination (e.g., stability protocol, COA for raw materials/bulk, micro-related checks, and third-party reports).
  • We do not guarantee regulatory approval, but we can help prepare the files and arrange send-out testing and report tracking as needed.
  • Operationally, our MOQ is typically 1000-3000 pcs (simple items may start at 1000; more complex sets often 3000).
  • After formula and sample confirmation, bulk lead time is usually 10-20 working days; packaging ordering is often 10-30 working days.
  • Common eye-cream packaging lead times: unit carton about 15 days; glass bottle 15 days; acrylic bottle 30 days; tube 15 days.
  • Full turnkey brand landing is generally 45-60 days depending on design and testing cadence.
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.
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  • Your information will be kept strictly confidential.

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