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Can you make fragrance-free eye cream for the U.S. market (and how do you manage odor)?

Yes-we can develop a fragrance-free eye cream for the U.S. market and manage odor through low-odor raw material selection, clean processing, and stable base design (no added perfume). We can also support testing and documentation to fit your compliance needs.

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.
  • We can formulate a fragrance-free eye cream (no added perfume) for sensitive-eye positioning.
  • Odor is managed by selecting naturally low-odor actives/emollients, controlling trace impurities, and keeping the base simple and stable; our manufacturing includes a medical-grade ultra-pure water system and automated ozone control to help keep the process clean.
  • If a faint raw-material note remains, we will tune the formula rather than masking it with fragrance.
  • MOQ is typically 1,000-3,000 units depending on formula and packaging complexity (simple formats can start at 1,000).
  • We support customized formula development and lab sampling, then you confirm the sample before mass production; for an overall one-stop brand launch, the typical end-to-end timeline is 45-60 days.
  • For compliance support, we can arrange product testing and track the inspection report, and provide factory documentation plus item barcode information.
  • Packaging can be coordinated with full VI/design support; typical packaging lead times include tube 15 days, glass bottle 15 days, acrylic bottle 30 days (packaging orders often take 10-30 working days).
  • After sample approval, bulk production is usually 10-20 working 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.

Request received

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