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How do you prevent leakage and cap loosening for eye serum droppers in U.S. shipping?

For US shipping (Amazon/FBA), we prevent eye serum dropper leakage by controlling the closure system (fit, torque, liner) and adding secondary tamper/leak protection. We can validate with leak + transport-simulation tests before mass production.

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 droppers, leakage and cap loosening usually come from mismatch between bottle neck finish and closure, insufficient cap torque, or no secondary seal.
  • We typically lock the system by confirming the bottle/closure spec (glass or acrylic), setting a torque standard during filling, and using a suitable liner/wiper insert.
  • For transit protection, we recommend a tamper-evident band or secondary sealing method plus a tight inner tray so the dropper is not side-loaded.
  • For Amazon US shipping, we also design the pack-out: individual unit protection (polybag or sleeve), divider/tray to keep droppers upright, and a stronger master carton to reduce vibration.
  • We can support packaging design and matching services, plus arrange packaging checks (typical packaging testing lead time is 3 days) and product send-out testing with report tracking.
  • MOQ is typically 1000-3000 pcs (simple items can start at 1000).
  • After sample confirmation, mass production lead time is usually 10-20 working days.
  • Packaging ordering often takes 10-30 working days (e.g., glass bottle 15 days, acrylic 30 days; single box 15 days, set box 20 days), so we plan both streams in parallel to reduce risk.
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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