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.
- OEM fragrance development starts with your brief, creating a unique formula through our R&D process.
- Private label selects from our existing portfolio with minimal changes.
- For US market, both require FDA registration and IFRA compliance documentation.
- OEM typically has 5,000+ unit MOQ and 8-12 week sampling timeline.
- Private label can start at 1,000 units with 2-4 week sampling.
- We provide stability testing, MSDS, and allergen documentation for both paths.
- Packaging customization options differ significantly between these models.
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.
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This page is a practical buyer guide. For definitive requirements and updates, use FDA resources and qualified regulatory counsel.