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USANA and High-Quality Manufacturing

USANA was founded with a mission to manufacture the highest-quality products without compromise—products people can trust. Because poor manufacturing can destroy great science, USANA is one of the few companies to manufacture most of its products in its own state-of-the-art facility.

To ensure that the formulas developed in USANA's laboratories are produced consistently, the same process is followed each time manufacturing begins.

Nutritionals You Can Trust
Each dietary supplement produced by USANA carries a Potency Guarantee, which ensures that what is stated on the label is actually contained in the product. 

USANA® Essentials™ (Mega Antioxidant and Chelated Mineral), Procosa® IIActive Calcium™, and theHealthPak™ have all been exhaustively tested by NSF International and have been found to contain all ingredients at the labeled amounts. NSF is an independent, not-for-profit organization that helps protect consumers by certifying products and writing standards for food, water, and consumer goods. 

In addition, when compared to 1,500 other products, USANA was named Editor’s Choice, and two products (Essentials and HealthPak) each received a top 5-star rating and Gold Medal of Achievement from NutriSearch Comparative Guide to Nutritional Supplements™, Consumer Edition

A number of USANA supplements have been evaluated and approved by ConsumerLab.com, a leading provider of independent test results and information. 

USANA is a member of the United Natural Products Alliance (UNPA)—an association of dietary supplement and functional food companies that share a commitment to provide consumers with natural health products of superior quality, benefit, and reliability. 

A Commitment to Strict Manufacturing Standards
The Food and Drug Administration requires that dietary supplement manufacturers follow Good Manufacturing Practices (GMP) for dietary supplements (21 CFR, part 111). USANA, however, voluntarily follows the more stringent GMP for pharmaceuticals as the basis for its quality assurance program, which regulates virtually every aspect of manufacturing, including facility design and maintenance, raw material specification and control, supplier validation, product design and testing, and more. This voluntary adherence to GMP for pharmaceuticals means that USANA treats nutritional supplements with the same care that goes into the manufacturing of over-the-counter products.

In addition, USANA has acquired Drug Establishment Registration with the U.S. Food and Drug Administration. This means USANA operates an FDA-registered facility, following the FDA’s highest possible standard for manufacturers. 

Also, where applicable, USANA voluntarily tests its supplements to make sure they meet trusted United States Pharmacopeia (USP) standards and specifications for potency, uniformity, and disintegration. 

In several countries around the world, supplements are more highly regulated than in the United States. In Australia, for example, the Therapeutic Goods Administration (TGA) mandates that manufacturers follow a set of GMP identical to pharmaceutical GMP in the United States. As an Australian supplier, USANA is regularly inspected and audited by the TGA to ensure that their GMP standards are met. 

Aside from meeting the criteria of regular TGA audits, USANA has voluntarily obtained additional third-party verification of GMP status. Since 2006, USANA’s Salt Lake City, Utah, manufacturing facility has been certified to be in compliance with NSF/ANSI Dietary Supplement GMP requirements set forth by NSF International. According to NSF, "GMP registration reflects [a] continued commitment to ensuring quality and satisfaction and gives companies confidence that their organization operates in conformance to established GMP."

It is USANA's mission to develop and provide the highest-quality, science-based products. By rigorously testing each product for potency and purity and by following pharmaceutical GMP, USANA sets the standard for excellence in dietary supplement manufacturing. Once again, this is proof that USANA products are truly Nutritionals You Can Trust.

Nutritional Hybrid Technology
Based on an advanced tableting technology used by the pharmaceutical industry, USANA's innovative Nutritional Hybrid Technology (NHT) is a state-of-the-art approach to formula design and manufacturing. NHT features bilayer tableting: the separation of various formula ingredients into two distinct tablet layers. Now, for the first time, incompatible ingredients can be combined in a single tablet, and key nutritional ingredients can be visually highlighted in distinct tablet layers.
 


USANA's Nutritional Hybrid Technology opens the door to accelerated innovation in supplement design and manufacture. The possibility of combining two existing products into one will allow us to simplify your daily nutrition routine by reducing the number of tablets that you have to take every day. And NHT has applications in sustained nutrient release, making it possible for us to design products that will deliver nutrients both quickly and over time.  

As a leader in nutritional innovation, USANA is proud to be one of the first in the industry to utilize it.


What USANA products use Nutritional Hybrid Technology?
US products listed. Products will vary by market.

USANA’s Hybrid pill Proflavanol® C100 combines powerful bioflavonoids from grape-seed extract on one side and our exclusive high-potency Poly C® on the other.  

Hepasil DTX® combines alpha-lipoic acid on one side and a proprietary blend of antioxidants, including our patented Olivol®, on the other.

 

*These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent diseases.

 

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