Our services include product chemistry formulation and De-formulation Analysis, Finished-Product Efficacy Testing, Ingredient Percentage Assay, and shelf-life testing.
We submit your products to FDA approval and NDC number assignment, Our minimum quantity for contract manufacturing of any drug product is 20,000pcs per line. Our lead period is 21 days. Topical treatments we manufacture using FDA approve monographs are Acne treatments, Antifungals, Antibiotics, Dandruff, External analgesics, and Skin bleaching gels., As part of our mission to contribute to human health, we also offer select ingredients derived from natural sources that are safe, effective, and cost-competitive.
Contact us for more details.