Preservatives and humectants shipped worldwide from Huaibei Anhui China
Supplier audit, batch testing, standards alignment and a document pack prepared for your destination market. This is the process behind every drum we ship.
We partner only with manufacturers who have proven track records and modern facilities. The audit is a precondition of the first order.
Certificates of Analysis are provided for every shipment, so the values your incoming inspection checks belong to the lot in front of it.
Our products are produced to meet relevant standards such as ISO, USP, EP and cosmetic requirements where applicable.
Issued for every batch shipped, listing the tested values for that lot.
Prepared in the format required by your destination market.
Issued for customs clearance in the importing country.
Invoice, packing list and shipping paperwork prepared with the shipment.
Purity grade, appearance, packaging and recommended usage range.
We stay informed about global regulatory landscapes, including the EU Cosmetic Regulation, the FDA and China NMPA, to help you navigate compliance requirements for your target markets.
In practice that means the dosage ceiling that applies to your category is stated in writing at the quotation stage, not discovered during registration. Phenoxyethanol at 1.0 percent, or 0.4 percent for products for children under three years, is the clearest example of a limit that decides a formulation before it is written.
Yes. Certificates of Analysis are provided for every shipment, tied to the batch you receive rather than to the product in general.
Products are produced to meet relevant standards such as ISO, USP, EP and cosmetic requirements where applicable. The applicable standard is stated per product.
We partner only with manufacturers that have proven track records and modern facilities, and the audit happens before your order is placed.
We stay informed about global regulatory landscapes such as the EU Cosmetic Regulation, the FDA and China NMPA, and we prepare documentation to suit. Registration itself is filed by the legal entity placing the product on that market.
Send us the incoming inspection result with the batch number. A discrepancy between the CoA and the delivered material is a supply failure on our side and is handled as one.
Name the ingredient and the destination market. The current specification, the sample CoA format and the SDS come back so your regulatory team can review before a purchase order.