Herbally Yours is contract manufacturer of nutritional supplements and personal care products.

New product development takes time. From initial contact we will work hard on research and development, to provide you first sample. From final sample first time orders usually take 6-8 weeks. We always strive to fulfill all orders within promised deadline.

No we can't. Since we are contract manufacturers we don't have a standard list of products. Each product is unique and specific for each customer, and we will never make same product for more than one customer. All of the formulas are confidential and never repeated.

Everywhere. One can search every story and will never find a product with Herbally Yours name printed on the label. We are manufacturer, that is what we do best.
But if you have purchased nutritional supplements in last 20 years, there is great chance that you already bought and enjoyed product made in our facility. From small mom-n-pop stores to any major chain store, from mail order catalogs to websites, our products are everywhere, and we always get excited to see product that left our production line somewhere on the store shelf.

We encounter this question often, and it is probably one of the hardest one to answer. We simply dont know, before knowing more about your product, packaging, certifications, marketing plan, investment, we cannot answer that question. Here at Herbally Yours, we understand the need for initial smaller runs to test the market, while being capable of large production runs.

Humonguous, all of them, but unfortunately we are not selling any of them.
However, we would love to give you a tour. Please visit our contact page and we will be more than happy to arrange tour for you, and your team.

Nope, FDA does not certify nutritional supplement manufacturers.

We are NSF cGMP certified, USDA Organic certified, Kosher certified, Halal certified, and Health Canada certified facility that is inspected by FDA.
We are FDA registered under Public Health Security and Bioterrorism Preparedness and Response Act of 2002 (the Bioterrorism Act), and FDA Food Safety Modernization Act (FSMA), enacted on January 4, 2011, which amended section 415 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), requiring facilities engaged in manufacturing, processing, packing, or holding food for consumption in the United States to submit additional registration information to FDA, including an assurance that FDA will be permitted to inspect the facility at the times and in the manner permitted by the FD&C Act.