cGMP Supplement Contract Manufacturing in Southern Utah

Supplement contract manufacturing means a brand hands formulation, production and packaging to a specialist manufacturer. The brand owns the product and the label. The manufacturer makes it to spec in a cGMP-compliant facility. Vitalpax is that partner for supplement brands, from concept to shelf.

Vitalpax manufactures capsules, tablets (standard and chewable), powders, single-serve sachets and stick packs, and liquids. Liquids include tinctures, herbal liquids, syrups, functional blends, liposomal products, probiotics and vitamins, in fills from 1 oz to 32 oz.

Yes. Vitalpax manufactures dietary supplements in a cGMP-compliant facility in Southern Utah. Quality is built into each step of the process, not added at the end.

Yes. Vitalpax manufactures private label supplements for DTC brands, Amazon sellers and distributors, and helps take a product from formulation to finished, packaged goods.

Vitalpax operates a multi-building manufacturing campus in La Verkin, in Southern Utah, USA.

Yes. Vitalpax supplies U.S.-made supplements to distributors and buyers outside the United States, and its product catalog is available in English, Arabic and Spanish.

Fill in the Get Customer Quote form on this site or call +1 866 848 2588. Share your formula or concept, format and target quantity. The details at the start matter.

Both. We can develop a custom formula from your brief or provide ready-to-brand options that can be modified to your specification.

For true custom development, you retain ownership of your formula once the project is completed and any development fees are settled. We maintain technical files for manufacturing and quality records only.

Yes, within regulatory and IP boundaries. We analyze label disclosures and use R&D best practices to create a functionally comparable formula.

Yes. A finished-product CoA is issued per lot, reflecting the agreed specification and test results.

Yes. We review Supplement Facts, ingredient statements, and structure/function claims for U.S. dietary supplement regulations, and can flag items that may require legal or regulatory counsel.

MOQs vary by dosage form, packaging, and ingredient constraints. We'll discuss practical starting volumes during scoping so the project is efficient and repeatable.

Yes. Pilot or small-batch runs are available to de-risk scale-up, validate process parameters, and generate market test inventory.

We support bottles, tubs & jars, and pouches (including stick packs, sachets, and gusseted pouches) plus retail cartons and compliant case-packing per routing guides.