Exhibitor
Standards
I. INTRODUCTION
This document comprises New Hope Natural Media’s
exhibitor standards for NATURAL PRODUCTS EXPO EAST and EXPO
WEST. This is a working document which is open at all times
to industry comment and review. As producers of two major,
national trade shows, New Hope Natural Media has the responsibility
to require minimum standards to exhibit at our EXPOs. In addition,
it is our hope that these standards will become part of the
overall effort to improve the quality and integrity of the
natural products industry.
Exhibitors are encouraged to review the entire document. Exhibitors
should be aware that they have signed a contract stating they
have read, understand and agree to abide by New Hope Natural
Media’s Exhibitor Standards. As stated in the Exhibitor Contract,
“New Hope Natural Media reserves the right to determine the
eligibility of any company or product for inclusion in its
trade shows.”
Statement
of Purpose
With these standards, it is New Hope Natural Media’s goal
to enhance public health and safety, support industry self-regulation,
improve the quality of natural products, and grow the industry
in a responsible way. These standards also represent New Hope
Natural Media’s attempt to raise the level of integrity and
professionalism of the EXPOs.
PERTINENT INFORMATION
A.
These standards cover six areas of focus:
1.
Product Safety
2. Product Ingredients
3. Product Claims
4. Product Labeling
5. Product Literature
6. Show Floor Activities
For
the purposes of these Standards, NATURAL PRODUCTS EXPOs
will distinguish between labels and labeling, and literature.
Labels and labeling include all packaging and any promotional
materials, brochures or other written materials used in
the sale of the product. Literature includes advertisements,
magazine articles, books and other printed, verbal or
visual matter that may or may not be about the product
but is not physically attached to the product.
B.
Standards and Guidelines
Each subsection contains Standards and Guidelines. Standards
are minimum requirements exhibitors must meet to participate
in a NATURAL PRODUCTS EXPO. Guidelines are recommendations
at this time but represent long-term goals to raise the
industry’s integrity. In the event an EXPO standard is
not as stringent or is in conflict with an applicable
government regulation, the government regulation will
take precedent.
C. Working with the Industry
New Hope Natural Media views these standards as part of
the larger industry effort designed to improve the health
of the American people, and to ensure the safety and accuracy
of information, and the integrity of natural products.
We intend to work with industry manufacturers, distributors,
brokers and retailers in addition to trade associations
and other organizations in a joint effort to accomplish
these goals.
D. Comments, Suggestions and Concerns
This is a working document. We encourage comments, suggestions and concerns from industry members and groups because it is our intention to provide standards that are fair, reasonable, concise and understandable. These standards will be updated and refined as necessary and will be appropriately revised to reflect the dynamic regulatory environment. Exhibitors will have ample time to correct any problems and respond to informational requests unless New Hope Natural Media perceives a situation that truly compromises consumer safety or jeopardizes the industry's or New Hope Natural Media's integrity. Please submit all questions or comments IN WRITING to New Hope Natural Media, Standards Committee, 1401 Pearl Street Suite 200, Boulder, CO 80302.
IMPLEMENTATION PLAN
These
standards are for NATURAL PRODUCTS EXPOs only. Compliance
with these standards does not exempt exhibitors from complying
with applicable legal or industry standards set forth by
organizations such as the Food and Drug Administration,
the Federal Trade Commission, the National Nutritional Foods
Association, the Organic Trade Association, or the American
Herbal Products Association. In addition, these standards
do not constitute an approval system. New Hope Natural Media
strives to collect and review all exhibit contents, but
makes no guarantees that every potential deviation from
Expo standards will be identified and communicated to exhibitors.
• Exhibitors are responsible for knowing and complying with
all standards.
• New Hope Natural Media reserves the right to determine
the eligibility of any company or product for inclusion
in its trade shows, as stated in the Exhibitor Contract.
A.
Implementation
1.
Literature and samples will be collected from exhibits. Exhibitors whose materials are deemed out of compliance may be notified. Lack of notification for noncompliance does not automatically signify compliance with NATURAL PRODUCTS EXPO standards.
2. The content of each exhibit will be considered on a case-by-case basis. Exhibitors are solely responsible for responding within the established deadlines for compliance.
3. Exhibitors will have ample time to correct any problems and respond to informational requests unless NATURAL PRODUCTS EXPO perceives a situation that truly compromises consumer safety or jeopardizes the industry's or New Hope Natural Media's integrity. In such an instance, an exhibitor may be asked to remove any contents from the exhibit immediately.
4. Pre-approval through the submission of labels, literature, and other materials will be required of new exhibitors who are not currently in compliance with established standards. Any exhibitor may be asked to submit materials intended as exhibit content for pre-approval, solely at the discretion of NATURAL PRODUCTS EXPO.
5. Acceptance for the materials reviewed for exhibit at Natural Products Tradeshows or Publications does not constitute a legal review for compliance with applicable FDA/FTC regulations.
6. As this document is further evaluated and refined,
exhibitors can expect enhanced enforcement at future EXPOs.
NATURAL PRODUCTS EXPO will keep exhibitors advised of
any changes.
1.
PRODUCT SAFETY
PURPOSE:
To ensure the safety of products and
services.
SECTION 1.A
Product
Safety / Directions and Warnings / Standards:
1. Products or services in the exhibit must be
safe as labeled for intended use.
2. Products that could be unsafe if used improperly
must identify directions for safe use and warnings against
misuse.
3. Products which are sold as over-the-counter
drugs must be labeled with appropriate consumer warnings
as specified in the appropriate OTC monograph.
4. Appropriate warning statements must be noted
for products which may be unsafe if consumed by certain
subpopulations. Examples: People with hypertension
or pregnant women.
Product Safety / Directions and Warnings
/ Guideline:
1. Tamper-evident packaging is encouraged along
with a clear description of the tamper-resistant features.
SECTION 1.B
Product
Safety / Child Safety / Standards:
1. Drugs or supplements manufactured and packaged
to appeal to children must have appropriate cautions or
warnings to prevent misuse by children.
2. Drugs or supplements packaged to appeal to children
must have child-resistant closures.
Product Safety / Child Safety / Guidelines:
1. All drugs and supplements should have appropriate
cautions and warnings to prevent misuse by children.
2. Tamper-resistant packaging or childresistant
closures as appropriate are encouraged for all drugs and
supplements.
3. Products that are unsafe or inappropriate for
use by children should not be packaged or marketed in
a manner that is targeted toward children or recognized
as candy by children.
4. Products that could be unsafe if consumed without
adult supervision should be clearly labeled as such.
SECTION 1.C
Product
Safety / Product Samples for Distribution on the Show
Floor / Standards:
1. All samples must include the following information:
name and address or phone number of manufacturer or distributor;
full labeling of ingredients; directions for use; warnings
against misuse if appropriate.
2. All dietary supplement samples must be packaged
in sealed units.
3. Exhibitors offering samples for immediate consumption
must provide a listing of ingredients and other relevant
information required by these standards in a location
that is easily visible to EXPO attendees.
4. All samples must be processed, prepared and
presented in a safe and sanitary manner according to federal,
state and local codes.
Product
Safety / Product Samples for Distribution on the Show
Floor / Guidelines:
1. Labels of product samples should be clearly
marked to designate the products not intended for resale.
2. Samples should carry a meaningful lot number
or other tracking mechanism.
2.
PRODUCT INGREDIENTS
SECTION 2.A
Product
Ingredients / Disclosure of Active Ingredients / Guideline:
1. Laxatives, stimulants and bronchodilators should
be clearly identified in literature and labeling.
SECTION 2.B
Product Ingredients / Quantitative Potency
Statements / Standards:
1. Products claiming a specific amount of a dietary
ingredient or a specific potency (with the exception of
homeopathic products) must be tested to ensure that statements
are accurate.
2. Products with a claimed potency (with the exception
of homeopathic products) must bear an open coded expiration
or “best if used by” date.
3. A declared potency must be accurate until the
expiration date.
4. If a declared potency is dependent on specialized
storage conditions, those conditions, the potency declared
and an expiration date or “best before” date must be listed.
5. Potency terminology must be easily understood
by a lay person with one exception: Homeopathic products
may declare potency or dilution using methods outlined
in the Homeopathic Pharmacopoeia of the United States.
6. Standardized potency statements must note the
chemical compound, compounds or class of compounds used
as the marker(s) for standardization, and how much of
that compound is present by weight, ratio or content as
a percentage.
Product
Ingredients / Quantitative Potency Statements / Guideline:
1. Extracts should state the equivalent weight of
starting material per volume or weight of extract.
SECTION 2.C
Product Ingredients / Basis of Formulation / Standard:
1. Homeopathic products must comply with the Homeopathic
Pharmacopoeia of the United States and the FDA Compliance
Guide, 7231.15, “Conditions under which Homeopathic Medicines
May Be Marketed.”
Product
Ingredients / Basis of Formulation / Guidelines:
1. Products formulated using
a specific philosophy should state that philosophy and
conform to that basis of formulation. Example:
“A traditional Chinese formula.”
2. Products claiming to be “ancient” formulas should
have documentation to support the claim and contain only
those ingredients originally included in the “ancient”
formula.
3. Ancient formulas combined with modern ingredients
should disclose these modifications to the original formula.
SECTION 2.D
Product
Ingredients / Natural Flavors and Essential Oils / Standards:
1. If the name of a fruit, spice, essential oil,
or other flavor or fragrance is part of a product title,
then that product must contain that substance. If it does
not, a disclaimer must appear directly under the product
title as specified by FDA regulations.
2. If the product contains only the essence of
a flavor, then the word “flavored”should be an integral
part of the product’s description.
3. If the flavoring agent comes from an artificial
source, the product must be labeled “artificially flavored."
4. Fruit drinks must state the content percentage
of real fruit juice as specified by FDA regulations.
5. Labeling of flavor ingredients must be in compliance
with applicable FDA regulations.
Product Ingredients / Natural Flavors
and Essential Oils / Guideline:
1. Essential oils not extracted from a plant
should be described as “artificial” or “synthetic.” Descriptors
such as “fragrance” or “essence” are not adequate.
SECTION 2.E
Product Ingredients / Endangered Plants and Animals /
Standard:
1. Products consisting of or containing any ingredients
derived from threatened or endangered plant or animal
species are not permitted in any EXPO exhibit. Promotional
literature offering such products is also disallowed.
SECTION 2.F
Product Ingredients / Common Names / Standard:
1. Product ingredients must be described by their
common or usual names, except for homeopathic products
which must be labeled with the Latin binomial.
SECTION 2.G
Product Ingredients / Nutrition Labeling / Standard:
1.
Conventional food products and dietary supplements must
comply with current FDA regulations for nutrition labeling
and nutrient content unless otherwise exempted.
SECTION 2.H
Product Ingredients / Not Allowed / Artificial Sweeteners / Foods / Standard:
1. The following sweeteners are synthetic, do not occur in nature, and will not be allowed in products and packaging labeled as food (products with a “Nutrition Facts” panel) for exhibit on the tradeshow floor:
Sucralose
Splenda®
Nutrasweet®
Equal®
Aspartame
Acesulfame potassium
Ace-K
Sunett®
Saccharin
Sweet ‘N Low®
Neotame
Product Ingredients / Not Allowed / Artificial Colorings / Foods / Guideline:
1. Natural foods should not contain any artificial colors. See the Natural Products Expo Ingredient Standards and Guidance document for a list of artificial colors and acceptable natural colors.
Product Ingredients / Not Allowed / Artificial Preservatives / Foods / Guideline:
1. Natural foods should not contain any artificial preservatives. See the Natural Products Expo Ingredient Standards and Guidance document for a list of artificial preservatives and acceptable natural preservatives.
Product Ingredients / Not Allowed / Artificial Flavorings / Foods / Guideline:
1. Natural foods should not contain any artificial flavorings. See the Natural Products Expo Ingredient Standards and Guidance document for a list of artificial flavorings and acceptable natural flavorings.
3. PRODUCT
CLAIMS
PURPOSES:
To ensure the truthfulness and accuracy of product statements.
To ensure substantiation and traceability of product statements.
To promote thorough understanding and knowledge of products
and product statements.
To promote equal evaluation and comparison of like products.
To preserve the integrity and meaning of legitimate statements
such as: “organically grown & certified organic,” “cruelty
free,” “recycled” and “historical formula.”
SECTION
3.A
Product Claims / Substantiation of Health Benefit or
Nutrient Content Statements / Standards:
1.
Exhibitors must provide substantiation of health benefit
statements, whether express, implied or contained in
product names. Adequate substantiation, including (but
not limited to), copies of complete published scientific
studies with journal name, date, volume and authors'
names must be provided at the request of a designated
New Hope Natural Media representative.
2. A bibliography of research will not generally
be adequate, unless it is accompanied by the above documentation.
3. Exhibitors must provide substantiation of
nutrient or ingredient content claims, which may consist
of a certificate of analysis or analytical results from
a qualified testing laboratory.
4. Testing must follow good laboratory practices
including method validation, calibration and confirmation
by an independent (FDA-registered if possible) laboratory.
Product
Claims / Substantiation of Health Benefit Statements /
Guidelines:
1. Exhibitors are encouraged to
provide and have available substantiation of all health
benefit statements or ingredient content statements
to any EXPO attendee.
2. All testing to validate health benefit statements
or ingredient content statements should be performed
by an independent, certified laboratory with published
Good Laboratory Practices.
SECTION
3.B
Product Claims / Superlative Statements / Guidelines:
1.
Superlative statements should only be made if they are
true, and the exhibitor has substantiation of such statements.
Examples: Superlative statements include (but
not limited to): "best in the world," "best
product in the U.S.," "only the finest herbs,"
"only the purest water," "the only,"
"the most potent" and "the most effective."
2. Superlative statements should not be misleading.
SECTION
3.C
Product Claims / Personnel or Process Statements /
Standards:
1. Individuals presented as doctors
must have a full and accurate title such as N.D., M.D.,
Ph.D., D.Ed., O.M.D. Such individuals must disclose details
of their education and training at the request of a designated
New Hope Natural Media representative.
2. Titles and initials must be stated clearly and,
if not commonly known, must be spelled out or explained.
3. Statements about facilities, staff, quality
control procedures, manufacturing processes or testing
must not be overstated. Proof of such practices or test
results must be supplied at the request of a designated
New Hope Natural Media representative.
4. Statements about institutions of higher education
must be truthful, not misleading and must disclose the
following information:
A. The accrediting agency/agencies
of the institution program stated.
B. Whether the accrediting agency/agencies
are recognized by the U.S. Secretary of Education.
C. If the degree or credentials
offered are recognized by other institutions of higher
education.
D. Whether the degree or credential
qualify the recipient to take state board exams in states
where licensing is required.
SECTION
3.D
Product Claims / Disease or Health Benefit Statement
/ Standards:
In accordance with the Dietary Supplement Health and Education Act of 1994 (DSHEA), and the U.S. Food, Drug and Cosmetic Act, dietary supplement, food and cosmetic products and their labeling must not claim to treat, prevent, mitigate, cure or reduce the risk of diseases, unless the complete FDA-approved unqualified or qualified health claim is used on the labeling.
The FDA considers that if a statement about a product or ingredient, claims to diagnose, mitigate, treat, cure, or prevent disease or if it has an effect on a specific disease, class of diseases or on the characteristic signs or symptoms of a disease, the product will be subject to regulation as a drug unless the claim is an authorized health claim for which the product qualifies.
1. Product labeling including sales and marketing material must not express or imply claims to diagnose, treat, cure, prevent or mitigate any diseases, including (but not limited to), cancer, heart disease, AIDS, diabetes, Alzheimer's disease, etc.
2. Substantial scientific data, to be determined
at the discretion of a New Hope Natural Media representative,
will be required to support benefit statements pertaining
to such diseases. The data if published must include
journal name, date, volume and authors' names.
SECTION
3.E
Product Claims / Organic Statements / Standards:
1.
“Organic” must be used truthfully in all statements.
2. All organic ingredient, product and production statements must have current USDA-accredited, third-party certification for compliance with the USDA's National Organic Program or other internationally recognized organic certification program.
3. Exhibitors claiming "certified"
organically grown or processed must have on file the
appropriate certification documents, and such documentation
must be available at the request of a New Hope Natural
Media representative.
Product
Claims / Organic Statements / Guidelines:
1.
Exhibitors should provide substantiation of organic
statements at the request of any EXPO attendee.
2. Organic certification documents should be
freely available on request. Labels and literature should
offer this documentation to consumers.
SECTION
3.F
Product Claims / Pesticide Free Statements / Standard:
1. Statements such as “pesticide
free,” “unsprayed" and “herbacide free” must be
documented. Information supporting such statements must
be available at the request of a designated New Hope
Natural Media representative.
SECTION
3.G
Product Claims / “No” and “Free” Statements / Standards:
1.
“No,” “low,” “lite” and “free” statements must comply
with all applicable FDA and FTC regulations.
2. Such statements must not be deceptive and
must fully disclose relevant facts. Examples: A statement
of “no salt added” is deceptive if the product contains
a high amount of sodium from hydrolyzed vegetable protein.
“No oil” is deceptive when the product is naturally
high in fat such as peanuts.
3. Products stating to be free of ingredients
with a particular activity must disclose the presence
of ingredients with similar activity. Example:
Products that contain no caffeine but do contain guarana.
4. Such statements must be substantiated with
documentation available at the request of a designated
New Hope Natural Media representative.
Product Claims / “No” and “Free” Statements
/ Guideline:
1.
If a product is said to be free of a substance that
actually remains in residual amounts, the residual amount
should be disclosed.
SECTION
3.H
Product Claims / Cruelty-Free Statements / Guidelines:
1. Products promoted as “cruelty
free” and “not tested on animals” should comply with
criteria established by such animal protection organizations
as PETA and NAVS.
2. Documentation of “cruelty free” and “not tested
on animals” statements should be available at the request
of a designated New Hope Natural Media representative.
SECTION 3.I
Product Claims / Recycled Statements / Standards:
1.
“Recycled” statements must be truthful and comply with
applicable parts of FTC and EPA regulations.
2. Recycled materials used in food packaging
must meet FDA regulations for food contact materials.
Product
Claims / Recycled Statements / Guideline:
1. "Recycled" statements
should be accurate and supported by a network of recycling
centers in the U.S.
SECTION
3.J
Product Claims / Charitable Contribution Statements /
Standard:
1.
Charitable contribution statements must be supported
by documentation and made available at the request of
a designated New Hope Natural Media representative.
SECTION 3.K
Product Claims / Statements Involving Testing / Standards:
1.
Test results referred to in promotional literature must
be made available at the request of a designated New
Hope Natural Media representative.
2. Testing statements must be significant and
relevant and not confusing or deceptive.
3. Statements and conclusions made about test
results must be logically derived from and supported
by test data.
4. Photos and data derived from tests including
stylistic or artistic renditions must be accurately
and objectively labeled and interpreted.
5. Promotional literature must state if the test
was conducted by an FDA-registered or certified independent
laboratory or by the promoter of the claim.
Product
Claims / Statements Involving Testing / Guidelines:
1.
Promotional literature should cite the test method and
the laboratory conducting the test.
2. Exhibitors are encouraged to provide test
results to any EXPO attendee on request.
3. Exhibitors should disclose the source of funding
for any tests cited.
SECTION
3.L
Product Claims / Disallowed Statements / Standard:
1.
The following products may not be exhibited at Expo:
• Alternatives to street drugs
• Recreational euphoriants/stimulants
• Sexual stimulants/enhancers (reviewed on a case-by-case
basis)
• Remedies for nuclear, biological, or chemical contaminants.
2.
Natural Products Expo evaluates all promotional literature
and/or labeling as a whole, including text, product
names and images used. Natural Products Expo allows
products that support natural sexual function, but not
those that seek to enhance sexual pleasure, endurance
or those marketed as aphrodisiacs.
3.
New Hope Natural Media strictly prohibits the exhibit,
advertising and promotion of products that claim to
protect against, detect, prevent or treat nuclear, biological
or chemical contaminants.
4.
PRODUCT LABEL REGULATORY COMPLIANCE
All
labels and labeling must be truthful and not misleading
and must comply with current FDA regulations.
5.
LABELS, LABELING AND LITERATURE
PURPOSES:
To ensure understanability and traceability of product
literature.
To promote equal evaluation and comparison of like products.
To ensure guarantees are fair and honored.
SECTION
5.A
Labels, Labeling and Literature / Names and Addresses
/ Standards:
1.
Product labels and promotional literature must include
the full name of the manufacturer or distributor and
mailing address.
2. Literature that does not list a trade name
must have the exhibitor’s name, city, state and zip
code and/or the phone number; or it must have the name
and address or phone number of the party responsible
for compilation and dissemination of the information.
Published “third-party literature” must bear a full
citation.
Labels,
Labeling and Literature / Phone Numbers / Guideline:
1. Product labels and promotional literature
should include a phone number for the manufacturer or
distributor.
SECTION
5.B
Labels, Labeling and Literature / Surveys / Standards:
1.
Survey statistics and conclusions must have a reference
that includes the following information:
• Methodology of survey
• Who conducted the survey
• The date the survey was conducted
• A written offer explaining how to obtain a copy
of the survey.
2.
Survey results must not be misrepresented.
Labels, Labeling and Literature / Surveys
/ Guideline:
1.
Surveys should contain the following information:
• Selection criteria for survey population
• Number of people surveyed
• Margin of error of the survey
• Source of funding for the survey.
SECTION
5.C
Labels, Labeling and Literature / Quotes / Standards:
1.
Quotes must not be misrepresented by being taken out
of context.
2. Endorsements by consumers must represent what
the typical experience of customers would be, not the
experience of just a few customers. Simply stating that
“Not all consumers will get these results” or “your
results may vary” is not enough.
3. Endorsement quotes must cite the speaker,
date and source of the quote.
SECTION
5.D
Labels, Labeling and Literature / Photos and Illustrations
/ Standards:
1.
Photos and illustrations may not be deceptive or
misleading.
2. Photos used in labeling and literature that
depict any aspect of a product’s processing, manufacture
or test must be of the manufacturer’s facility or accurately
labeled with the name of the Photos and Illustrations/Standards
facility pictured and its relationship to the exhibitor’s
product.
3. Before/after and comparison photos must be
used in the following manner:
•
Include a caption stating the time of the first photo
and the time of the second photo.
• Exposure and print techniques must be identical
for each photo.
4.
Photos and illustrations should not contain additional
misleading features or characteristics.
SECTION 5.E
Labels, Labeling and Literature / Art and Technical Terms
/ Standards:
1.
Artistic or contrived terms used in labeling and literature
must be understandable.
2. The use of a term must not differ from its
commonly accepted meaning.
Art
and Technical Terms / Guideline:
1. A coined term or descriptive
phrase should not be used to imply one product’s superiority
over another solely by virtue of the use of that coined
term or phrase.
Section
5.F
Labels, Labeling and Literature / Comparison and Negative
Advertising / Standard:
1.
All comparison and negative advertising must comply
with FTC regulations. FTC defines comparison advertising
as that which “compares alternative brands on objectively
measurable attributes or price and identifies the alternative
brand by name, illustration or other distinctive information.”
Labels,
Labeling and Literature / Comparison and Negative Advertising
/ Guidelines:
1.
Data cited should be made available on request to any
EXPO attendee.
2. Negative statements about companies or products
should be thoroughly documented and such documentation
made available at the request of a designated New Hope
Natural Media representative.
Section
5.G
Labels, Labeling and Literature / Guarantees / Standards:
1.
Guarantees must be easily understandable and must not
be misleading and must include relevant terms and conditions.
2. Companies offering guarantees must honor the
guarantee.
Section
5.H
Labels, Labeling and Literature / Use of Information
/ Standard:
1.
The exhibitor is responsible for the accuracy of all
information present in the booth that pertains to products
or services offered.
Labels, Labeling and Literature / Use
of Information / Guidelines:
1. Information that is primarily
educational and helps to better understand the product
is encouraged.
2. Information should state product limitations
and encourage an integrated approach to wellness using
a variety of techniques.
3. Information from an impartial third party
is encouraged.
4. Information about the cultural context of
use or philosophical basis of formulation is encouraged.
5. Information which addresses cultivation techniques
and ingredient and product processing methods is encouraged.
6. Information should explain technical terms
and cite references for any statements made.
6.
TRADE SHOW ACTIVITIES
PURPOSES:
To ensure EXPO attendees are not placed at risk by
unsafe practices by exhibitors and are properly informed.
To ensure compliance with exhibit
hall rules and local ordinances.
To encourage ethical behavior.
SECTION
6.A
Trade Show Activities / Medical Testing and Treatment
/ Standards:
1.
All medical testing, diagnosis and treatment conducted
within exhibits must be done by a qualified medical
practitioner.
2. The medical practitioner’s title and qualifications
must be prominently displayed.
3. Testing must be conducted in a safe manner.
4. Test or treatments resulting in medical waste
or which may contaminate attendees are strictly prohibited.
Example: Drawing blood or other bodily fluids;
the use of needles.
5. A written report stating the test’s validity
and usefulness must be available to attendees.
SECTION
6.B
Trade Show Activities / Product Manufacture and Preparation
/ Standards:
1.
Products or samples manufactured or prepared at EXPO
must comply with federal, state and local regulations
pertaining to food preparation.
2. Products or samples that cannot comply with
these regulations must not be offered for consumption
and may only be used for demonstration purposes.
SECTION
6.C
Trade Show Activities / Sale of Products / Standard:
1.
Food, beverages and other products intended for immediate
consumption must be offered free of charge.
SECTION
6.D
Trade Show Activities / Ethical Considerations / Guideline:
1.
Exhibitors are requested to adhere to ethical considerations
in areas including but not limited to the following:
• Racism
• Sexism
• Sexually explicit materials
• Animal Cruelty
• Decorum
• Environmental concerns.
SECTION
6.E
Trade Show Activities / Seminars / Standards:
1. Seminar speakers, including exhibitors and
representatives from companies who pay to give an Exhibitor
Presented Seminar at Natural Products Expo, must not
make defamatory, libelous or slanderous statements about
an exhibitor, company or person during a seminar.
2. Information given at seminars must be truthful
and non-misleading.
3 . Substantiation for claims and statements
made during seminars must be provided to a designated
New Hope Natural Media representative on request.
APPENDIX
GUIDELINE:
Not mandatory at this time but represent long-term goals to
raise the industry’s integrity.
HEALTH
BENEFIT STATEMENT: A statement which identifies a potential
benefit to health from a product. This is not to be construed
to mean a drug claim, a NLEA health claim, or a DSHEA statement
of nutritional support.
LABELS:
Include all packaging and any written materials attached to
or accompanying the product.
LABELING: Includes all packaging, promotional
materials, brochures, and any other written materials attached
to or accompanying the product; verbal or visual representations
including video, audio- tapes and signage.
LITERATURE:
Includes promotional materials, advertisements, brochures,
magazine articles, books and other printed matter that may
or may not be about the product but is not physically attached
to the product.
ON
FILE: The company has substantiating information in its
records at its head- quarters and the information is easily
accessible upon request.
QUALIFIED
MEDICAL PRACTITIONER: A graduate of an accredited institution
of higher learning.
STANDARD: A minimum requirement exhibitors
must meet to participate in a NATURAL PRODUCTS EXPO.
GLOSSARY OF ACRONYMS
EPA
Environmental Protection Agency www.epa.gov
FTC
Fedral Trade Commission www.ftc.gov
FDA Food and Drug Administration www.fda.gov
HPUS Homeopathic Pharmacopoeia of the
United States www.hpus.com
NAVS
National Anti-vivisection Society www.navs.org
PETA
People for the Ethical Treatment of Animals www.peta-online.com
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