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 US market compliance, we commonly formulate with pyrithione zinc (0.3-1%), selenium sulfide (1%), salicylic acid (1.8-3%), ketoconazole (1%), and coal tar (0.5-5%).
- Our MOQ starts at 3,000 units for standard formats.
- Sampling takes 4-6 weeks including stability testing.
- We provide full documentation including ingredient specifications and safety data.
- Packaging must consider active compatibility with materials to prevent leaching.
- Production lead time is 8-12 weeks after formula approval.
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.