The demand for mushroom based supplements continues to grow, however the number of products and product claims on the market make it hard for consumers to identify real markers of quality and function in many of the available brands.

 

 

The purpose of the Mushrooms-Plus line is to remove these uncertainties of quality and function, and to produce a line that will stand out as providing the very best health benefits to consumers, backed by clear, verified science.

 

 

EACH FORMULA IN THE LINE IS DEVELOPED WITH THE FOLLOWING QUALITIES:

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  • 100% organically certified mushroom extracts standardized for key active components such Beta-D-Glucans and ergothioneine.
  • No starch or fillers from mycelium-based ingredients: fruit body extracts only.
  • Extracts blended with key ingredients such as AlphaWave® L-Theanine, purified ergothioneine and PureLeaf® Ginkgo biloba extract to enhance S/F claims and increase benefits for the consumer.
  • Standardized extracts are sourced though NAMMEX then blended and tested at ENI’s cGMP facility.
  • Formulas are designed for effective dose to fit into 2 capsules per serving size and are available as powdered blends or finished products (encapsulated and bottled) under your brand.

 

 

LEARN MORE ABOUT OUR MUSHROOMS-PLUS PRODUCT LINE:

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ALL PRODUCTS AVAILABLE IN POWDER OR ENCAPSULATED FORM. CUSTOM BLENDS AVAILABLE.

The above statements have not been evaluated by the Food and Drug Administration.
This product is not intended to diagnose, treat, cure, or mitigate any disease.

 

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Ethical Naturals, Inc. (ENI)

 

CORPORATE OFFICE
18 Commercial Blvd.
Novato, CA 94949

This email address is being protected from spambots. You need JavaScript enabled to view it.
Tel: 866.459.4454 | 415.842.7687
Fax: 415.842.7682

Ethical Naturals, Inc. (ENI)

 

LOGISTICS/LABORATORY
2731 Fair Oaks Ave.
Redwood City, CA 94063

Tel: 650.336.1190
Fax: 650.336.1196

MEMBER/SUPPORTER OF:

 

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Ethical Naturals Inc., is certified to comply with NSF GMP Registration Program Requirements of NSF/ANSI 173, Section 8 which includes FSMA and cGMP (21 CFR 111), (21 CFR 117).

 
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