Dominican Republic 2009
Dominican Republic 2009
Dominican Republic 2009
Date: 7/31/2009
GAIN Report Number: DR9011
Dominican Republic
Approved By:
Jamie Rothschild, Agricultural Attaché
Prepared By:
Carlos G. Suarez, Ag Specialist
Report Highlights:
Sections updated: I Food Laws and Government regulatory agency contacts. Appendix V
Import Procedures.
Overall, the food laws in the Dominican Republic have not restricted trade for U.S. products.
There are four government Ministries involved in setting food policy for the country: the
Ministry of Health (Secretaría de Estado de Salud Pública y Asistencia Social - SESPAS), the
Ministry of Industry and Commerce (Secretaría de Estado de Industria y Comercio -SEI&C), the
Ministry of Agriculture (Secretaría de Estado de Agricultura – SEA) and the Ministry of the
Environment and Natural Resources (ME&NR). Nonetheless SESPAS plays a leading role within
the ministries.
The DR-CAFTA agreement implemented in March 1, 2007 provides the regulatory environment
and philosophy to help the country update its public its laws, regulations, procedures and
administrative rulings of general application respecting any matter covered by the Agreement
(CAFTA-DR Layman’s Guide, USAID). It is believed that the Agreement will help the country to
streamline procedures and update legislation which should facilitate trade for all partners.
The Environment and Food Control Division of Ministry of Public Health (SESPAS) is responsible
for implementing the General Health Law 42-01. This is a general food safety law and has
limited impact on U.S. food products exports. This law includes that all or imported products
must be registered. Product samples shipped via express mail or parcel post are not subject to
the registration process although they are subject to sanitary regulations and normal customs
procedures.
The specific sections in 42-01 which relate to food products are: Decree 2430 from 1984,
Ruling for meats and meat products for Export; Order 528-01, General Ruling for Risk Control
of Foods and Drinks in the Dominican Republic; and Order 2332, ruling for Hotels, Bars and
Restaurants. Currently, the Ministry is drafting degrees to cover an update on the meat law, a
second on poultry and poultry products, good manufacturing practices, and a third one on fish
and fish products. The update and the other two new draft laws have been sponsored by a
USAID contractor and are currently being submitted to the Congress.
SESPAS requires imported foodstuffs for consumer-ready foods and beverages sector to be
registered by domestically established companies. Their regulatory system implementation
mechanism is somewhat weak and is in the process of being improved, in order to expedite
registration procedure and to have more effective control on the new products being
marketed. SEI&C, DIGENOR in their implementation role in food labeling law, is moving along
to fully apply their labeling standard (NORDOM 53). Currently the focus has been mainly in
registration number of products and the Spanish language component within the labeling
requirement.
According to DIGENOR the basic labeling information must be in Spanish. This requirement has
created some marketing problems with labeled products from the United States with just an
English language label. More and more the multi language label has helped to overcome this
requirement. In the meantime, importers and distributors are using self adhesive labels (stick-
on labels) in Spanish at additional costs, to meet the Dominican Government labeling
requirement when the products from the United States do not arrive with Spanish labels.
The Biodiversity and Wildlife Division from ME&NR and the Ministry of Agriculture (SEA), Food
Safety Division play a minor role in rulemaking, although they are part of the “commission”
reviewing the scientific aspects as they relate to policy recommendations. The Ministry of
Agriculture is responsible for animal and plant health and also has a section for food safety.
Most of the challenges experienced by U.S. exporters relate to phytosanitary and zoo sanitary
issues.
A. General Requirements:
There is a general prepackaged food law which applies to local and imported food products
required prior to retail sale called NORDOM 53. It contains the labeling requirements of the
country. U.S. labels in food products can enter the country for relabeling before distribution.
The U.S. Labeling Standard meets most of the local ruling except for the language, weight units
and registration number. Stick-on labels are acceptable. There are no special labeling
requirements for sample-size products or institutional packed product destined for the food
service sector. The “best use before date” is required (day, month, year) is required but,
month, day year is readily acceptable. This ruling does not pertain to bulk commodities or
industrial packaged products.
The SEI&C, Norms and Standards Directorate currently have limited personnel resources to
assist the entity in fully implementing the labeling requirements throughout the country. They
have focused mainly in working at the primary source of entry (importers and distributors) to
supply products with labels in Spanish to their costumers. Importers and distributors are
already meeting this requirement to the wholesalers and supermarket chains in major cities.
With their resources, DIGENOR inspectors are not focused further down in the distribution
chain. With time, they will focus with other aspects of the labeling standard in order to have all
product labels of foodstuff for the consumer-ready food and beverage sector meet the standard
for both: imported and locally produced. This will be a slow process and it is not anticipated to
occur in the near future. The ruling gives the authority to DIGENOR to seize products at the
retail level when the products do not meet the requirements, but this action rarely takes place.
The office of the Norms and Standards Directorate (DIGENOR) of the Ministry of Industry and
Commerce and SESPAS are responsible for regulating this law. The regulation establishes the
mandatory requirements for labels of prepackaged individual and boxed foods. The label must
contain the following information: name, ingredients’ list, net & dry weights (in International
Units, such as: kg, ml, etc.), manufacturer name and address (manufacturer, processor,
importer, exporter or retailer), industrial and sanitary registration numbers (see Sanitary
Registration Procedure in Appendix IV), country of origin, lot number, and instructions for use.
The full text of NORDOM 53 is included in Appendix VI. The label must be in SPANISH –
stickers or multilingual labels are accepted. Please note U.S. labeling standards have been
accepted but the text should be reviewed as it basically follows the Codex Alimentarius
standard.
English labels have been accepted since the regulation was established about 10 years ago.
However, in November 2007, DIGENOR announced strict enforcement of NORDOM 53 where
the label must be in Spanish. This label must be applied prior to the point of sale at the retail
level. Bulk commodities, cosmetics, tobacco products, wine, and distilled spirits are exempted
from the Spanish labeling requirement.
U.S. standards of labeling have not being considered false or misleading in the Dominican
Republic. The DR generally shares and accepts the U.S. “Recommended Daily Intake (RDIs)”
standards from the United States. Shelf-life requirement have been occasionally questioned in
the past by Customs (yogurt’s short life), but accepted and shelf life information must be on
the label.
The standard U.S. nutritional fact panel is accepted and often used as a valid reference.
Ingredients are required but nutritional labeling table is preferred. It is a voluntary regulation,
but it is not mandatory. The details, such as saturated fats, fiber content, sodium content,
“light”, as the new necessities in health foods, etc., are not considered nor included in the
current requirement. The local authorities have informed us that they are considering
reviewing the current status and content of the standard for labeling. No tentative date has
been set nor programmed for this revision with the Ministries of Health and Industry and
Commerce.
The Government, within the Ministry of Public Health (SESPAS) has a Food Control Division and
it is responsible for claims at their legal department. These claims could be included as part of
the labeling when the product registration takes place. Nonetheless a new Division from the
Ministry of Industry and Commerce was recently created to deal with consumer protection
issues.
There are no special packaging requirements or preferences under the current ruling. As a
general rule, packing and container materials must be made of harmless material, free from
substances that could affect product safety. Likewise, packages must be manufactured to
preserve the product’s sanitation and composition throughout its useful life.
Specific container size is not regulated nor controlled by government authorities, the market
dictates preferences. Under the current regime, City Hall does not have any municipal waste
disposal laws in place, which impact imported products. In addition, there are no restrictions in
the use of any type of plastic, such as polyethylene, polypropylene, polyvinyl chloride nor any
other type of single or multi component synthetic packing material, although the contamination
level of this material in dumps, rivers and oceans is very high.
The Dominican Food regulation defines a “Food Additive” as any substance that is not
consumed normally for nutritional value, nor used as a typical ingredient in food, and does not
have any intrinsic nutritional value. The additive’s purpose in the product is to reach a state or
characteristic that the food does not naturally possess (such as enhanced color, taste, or shelf
life). Said additive could be included in the processing of the product or in the treatment of the
packaging. Also, if there is something in the manner of transporting or storing the product that
changes the chemical integrity of the product, it must be noted. This term does not refer to
contaminants or substances added to maintain or improve the nutritional value of the products.
The DR recognizes and accepts as safe the list from the CODEX and U.S. Standards approved
food additives and natural aromas for imported foodstuff. If a new additive is to be added to
the local additive list, DIGENOR at the corresponding technical committee has public forums,
defines a preliminary standard, and develops a norm.
DIGENOR, is engaged in the preparation of two new standards, NORDOM 622: Food Additives
and Contaminants which refers to labeling food additives for free sale and, NORDOM 623: Food
Additives and Contaminants on natural aromas. These refer to the general requirements and
do not include the authorized nor restricted natural aromas used as food ingredients. Therefore
tolerance levels for additives or aromas are included (Post has copies of both proposals and are
available in Spanish).
Registration requirements may be waived for products in transit, products used in research,
and products used to combat specific phytosanitary problems. The requirements and
procedures for registration, importation, exportation, production, storage, distribution,
transportation, repackaging, mixing, research, sale and use of these substances are described
in the Technical Regulations for each type of agricultural input, including pesticides, fertilizers,
biological and biochemical substances, and related agricultural substances (see registration
procedure in Appendix III).
The following laws, acts and decrees, which are the most important regulations concerning
pesticide use. They are contained in Law 311-68, SEA Regulation 322-88, Decree 217-91 with
prohibited products, and SEA Resolutions 10-97 and 11-97 as well as the General Health Law
42-01 and its orders. There are also a number of pesticides in a list of “probable restricted
pesticide use list” being debated at the Ministry. A list of approved pesticides can be obtained
from the Department of Plant Health (for address, see the contact section of this report).
Pesticide uses on agricultural products are contained under the Decree 52-08 on Good
Agricultural and Livestock and Manufacturing Practices. This decree is administered by the
Animal and Plant Food Safety Department (DIA) at the Ministry of Agriculture. This decree is
available upon request.
All companies and imported products are required to register with the Ministry of Industry and
Commerce and the Ministry of Public Health. The industrial registration number is required per
the labeling law (NORDOM 53). If forms are approved, registration should be completed within
5-20 days.
The Environmental Health Directorate of the Ministry of Public Health, orders that foreign
commercial food products in the country must be registered as required by Health Law 42-01
and Order 528-01: Food and Beverage Risk Control Unit. In addition to Certificate of Free sale
from the country of origin, the company must have a legal representative to which the
certificate will be issued. After all the required documentation is in place and a US$ 120 fee is
paid, a sanitary certificate will be issued within 30-90 days.
International Units are required. Nonetheless, units and measures used in the Dominican
Republic have not being standardized. Weight measures use pounds at the retail level, and
quintals (hundred weight – 100 lbs.) are frequently used as a wholesale unit. Metric tons and
kilos are used, but short tons (2,000 lbs.) are standard for sugar related use. Volume units,
such as gallons (3.8 liters), botellas (one quart), and cuartillos (pint) are often used. At the
same time, liters and cubic meters are found frequently. For linear measurements, although
the Dominican Republic uses metric system, it uses meters and feet units in construction.
Radiated Foods
Under the general labeling regulation (NORDOM 53), labels of products that have been
irradiated must indicate such treatment in a place near the product name. The use of the
international sign is optional, but whenever it is used, it must be placed near the product
name. When an irradiated product is used as an ingredient, it must be declared in the list of
ingredients. Also, when a product is made of only one ingredient and this is prepared with
irradiated raw materials, the undergone treatment must be specified on the label.
GMOs are accepted. Currently, there are no provisions in Dominican laws for genetically
modified products, although the Dominican Republic became signatory of the Cartagena
Protocol in early 2006. There are no regulations in place regarding Genetically Modified
Organisms (GMOs) neither from the Ministry of Environment nor from the Ministry of Public
Health.
A draft of the environmental law following CODEX standards is being considered for further
discussion.
Anyone who wishes to register a trade name or trademark must determine the availability of
the name or mark in the desired class with the Ministry of Industry and Commerce. If the
name is available, the Ministry will issue a certificate of availability, valid for 30 days, during
which the petitioner must apply for the desired registration. The applicant must submit an
application letter for registration to the Ministry. It must contain the petitioner’s name,
profession, address, and nationality. If the petitioner resides in the Dominican Republic,
identification card number or passport number is required. If the petitioner is a corporation,
this information must be submitted with respect to an official of the company.
When a legal representative submits the request, the information must be given for the legal
representative. If the power of attorney was granted abroad, a copy of the power of attorney
must accompany the application, duly certified by the authorities (nearest Dominican
Consulate).
The application, furthermore, must contain a detailed description of the following: (1) all the
elements that characterize the trademark or trade name being registered; (2) the type of
business for which the trademark or trade name will be used; (3) the products, goods or
business to which the mark or name will be applied; (4) the period of time for which the
petitioner wishes to register the mark or name. For registration of a trademark, the petitioner
must indicate the class corresponding to the product, according to the classification prescribed
in Law 20-00. This classification does not necessarily conform to the international classification
established by the Convention of Trademarks and Trade names.
The petition must be accompanied by four or more samples of facsimiles of the mark or name
being registered, together with a detailed explanation of what the mark or name is requested.
The petitioner cannot include in one registration application a name or mark that protects
different products.
Brand or name may be registered for ten years. Once a trade name or trademark is registered,
the petitioner is guaranteed the exclusive right to use the mark or name for the requested
period of time. This registration period can be extended or renewed for equal periods. There
are cases in which the name or trademark can be contested if improperly registered.
Secretariat of Agriculture,
For further information, check the FAS web site www.fas.usda.gov or our web site
www.usemb.gov.do/FAS. Please, also check other food market related reports for the
Dominican Republic including: the Exporter Guide; Food Processing Ingredients Sector; Retail
Food Sector and Hotel, Restaurant and Institutional Sector.
Author Defined:
Appendix III – PESTICIDE REGISTRATION PROCEDURE
In general, the Dominican Republic accepts United States and the European Union Standards
for Pesticides and other contaminants regulations. The Dominican Public Health Secretariat is
responsible for assuring that the Maximum Residue Levels (MRL) in foodstuff remains at
acceptable levels. Nonetheless, due to the limitations at the Secretariat and laboratories that
can perform such analysis, the regulatory frame is very weak.
Outside the Ministry of Agriculture, there is very little information on pesticides registration in
the Dominican Republic (only 5: Aldrin, Chlordane, Chlordimeform, Dieldrin and Heptachlor are
registered in an international database such as PAN Pesticide database). Nonetheless, the
Secretary of Agriculture (SEA) is responsible for registration of, manufacturing of, commercial
sales of and distribution of pesticides in the country. SEA internal Ruling 322-1988 Regulates
the Use and Control of pesticides contained in Law 311, which Regulates the Manufacturing,
Packaging, Storing, Importing and Commercial Sales of Pesticides and Similar Products, issued
on 22/05/1968. In 1995, the regulation was updated and resolution 4795 was effective
regarding the costs of registration.
Commercial and local manufactured pesticides must be registered at Pesticide Registration Unit
at the Plant Health Department, Secretary of Agriculture with appropriate documentation. The
company registration procedure can move in two directions: as a representative (no
warehouse) and as a distributor (warehouse and technical personnel).
A representation company must register for a fee (RD$ 12,500 or US$ 348 at an exchange rate
of RD$36/US$) with an appropriate form (documents include copies of the Company’s legal
constitutional credentials, Commercial Name registration from the Ministry of Industry and
Commerce and the represented Company information and affidavit and its legal representative
information [lawyer]) and then register the products individually for a five-year term. This
procedure requires 1-6 weeks. After the company’s has been registered, each product file has
to be deposited for a five-year period for a second fee a product fee of RD$5,000 or US$ 139 at
an exchange rate of RD$36/US, and half of this amount thereafter for the renewal of a five-
year term. The product registration fee with all the appropriate documentation in place takes
3-6 months to process.
In case of a distribution company for Importing or manufacturing pesticides (documents include
copies of the Company’s legal constitutional credentials, Commercial Name registration from
the Ministry of Industry and Commerce and the represented Company information and affidavit
and its legal representative information [lawyer] an information of their technical director),
again the company must register first as a pesticides supplier for a fee (US$ 173). This
procedure requires after all the required documentation, 3-6 weeks. After registering the
company, each product has to be registered for a five-year period for a second fee (US$ 139)
and half of this amount thereafter for the renewal of a five-year term. The product registration
fee with all the appropriate documentation in place takes 3-6 months to process.
All products for registration require laboratory testing. Due to local laboratory facilities
limitations, documentation to ensure conformity to import standards and test results is
generally sufficient to fulfill the requirements. For product sample shipments, upon company
request, Pesticide Registration Unit must issue an import authorization before arrival. This
document must be presented at customs before release of the samples.
In principle, the Pesticide Registration Unit should monitor the distribution at the
retail/wholesaler level, but due to infrastructure limitations, the ministry does it on a case-by-
case basis.
In order to commercialize food products and raw materials for the food industry in the
Dominican Republic, they must be registered at the Food and Beverage Control Department,
Environmental Health Directorate, Ministry of Health (SESPAS) (based on the General Health
Law 42-01 and its General Rule on Risk Control for Food and Beverages 528-01).
1) Permits
Animal products: The Livestock Department (DIGEGA), within the Secretary of Agriculture,
requires that the importer must request in writing a “non objection zoo certificate” (it would be
different for each individual commodity), indicating product quantity and origin of the
commodity to be imported. DIGEGA in turn classifies these products in “meats” and/or “dairy”
products and charge a fee per category. After obtaining the zoo permit, an additional request
must be made to the “Agricultural and Livestock Promotion Committee.” This committee is
headed by the Secretary of Agriculture who signs and issues this permit prior to the importation
of the animal product in question. There is also a fee for this requirement.
The fees for animal products are as follows: zoo permit per category (RD$2,000 or US$55.55
[or twice that amount if the two categories are within a permit request] at current exchange of
RD$36/US$) and an additional RD$2,000 for the other part of the permit.
Plant products: The Plant Health Department (PHD), within the Secretary of Agriculture,
requires that the importer must request in writing a “non objection phyto certificate” (it would
be different for each individual commodity), indicating product quantity and origin of the
commodity of products to be imported. The PHD charges a fee per request and points out the
individual product requirements (ie. Free of specific pests and or any other restrictions that
must be met prior to importation. After obtaining the phyto permit, an additional request must
be made to the “Agricultural and Livestock Promotion Committee.”
This committee is headed by the Secretary of Agriculture who signs and issues this permit prior
to the importation of the plant product in question. There is also a fee for this requirement.
The fees for plant products are as follows: phyto permit per request (RD$2,000 or US$55.55 at
current exchange of RD$36/US$) and an additional RD$2,000 for the other part of the permit.
It is important to note that the non-phyto/zoo permit is inconsistent with the DR-CAFTA
agreement. Nonetheless, for DR-CAFTA tariff rate quotas, a different permit is issued at the
time of the allocation without charges.
2) Import procedure
After the documents are issued, importers must obtain from their suppliers a USDA certificate
(APHIS VS 16-4 veterinary certificate) and it must include all the requirements stated in the
“non objection phyto and/or zoo certificate” (it would be different for each individual
commodity).
Occasionally the heat treatment statement has been required for new products in addition to
the health certificate. If required, the certification can be provided by the manufacturer on
company letterhead, and does not need to be certified by USDA.
The DR requires legalization at the DR Consulate of all documents except the Commercial
Invoice, Packing List and Bill of Lading.
The current national standard (NORDOM 53) labeling requirement, which is in place and begun
enforced on November 21, 2007, requires Spanish language and must include the following:
1. Food Name
a) The name of the product must indicate its true nature, and usually should be specific, not
generic.
When, according to the Codex or to a national norm, there are several names for the same
product, at least one of these names must be used.
In other cases, the name prescribed by the National Legislation must be used.
When the above names are not available a common name should be used, as long as it does
not deceive the consumer.
In the label, any phrase or sentence needed to clarify the nature of the product, such as kind of
covering, presentation of the product or any special treatment (like dehydration, reconstitution
or smoked), must be placed close to the name of the product.
2. Ingredients list
In all cases, except when the product has only one ingredient, an ingredient list must appear in
the label.
The list must have an appropriate title with the word "ingredient" included.
The ingredient list should be given, in a decreasing order, by the weight of the ingredient, when
the food was manufactured.
When an ingredient is a combination of two or more product additives, this ingredient
(compound ingredient) can be listed as one, as long as it goes with a list (in parenthesis) of its
individual constituents in decreasing order of proportions. When a compound ingredient, which
has a name from the Codex or from a national norm, has a 25 percent share (or less) of the
total product, its ingredient list does not need to be specified, except for the food additives that
have a technological function in the final product.
If water is added, it must be indicated in the list of ingredients, except when the water is part
of ingredients, such as broth in a food product, and declared as such in the list of ingredients.
It is not necessary to declare water or other volatile ingredients that may evaporate during the
production process.
As an alternative to the general dispositions of this section, for dehydrated or condensed foods
destined for reconstitution, the ingredients can be listed by order of proportions in the
reconstituted product, as long as the list includes a sentence, such as "Product ingredients
when prepared following the instructions on the label."
The following generic names for the ingredients that belong to the corresponding classes can be
used (see standard).
As an exemption, the following products must be specified by their specific names: pork fat,
butter and bovine fat.
When listing food additives belonging to different classes, the following generic names
(together with the specific name according to the Codex or to the National Legislation) must be
used: Agglutinant(s); Antioxidant(s); Dyes(s); Emulsifier(s); Aroma enhancer(s); Glossy
agent(s); Preserving substance(s); Stabilizer(s); Thickener/gel agent(s); Antisparkling(s); Flour
treatment agent(s); Artificial sweetener(s); Acidity regulator(s); Propellant(s); Yeast(s); and
Emulsifier salt (Only in case of melted cheese and its by-products).
For food additives belonging to the same class, which are listed in the Codex and authorized for
use, the following generic names can be used (a new norm is being drafted to include these
products (NORDOM 622).
Aroma(s) Chemically modified starch. The "aromas" can be classified as: naturals, similar to
naturals, artificial or a mix of them. A new norm is being drafted (NORDOM 623)
Food Preparation, cooperator and food additive transfer. Any food additive that has been used
as a part of the ingredients of a compound ingredient or in the product's raw materials, and
that has a technological effect in the final product, must be included in the list of ingredients.
The food additives transferred to the food in small quantities, and the elaboration should be
completed properly.
3. Net weight and drained weight
The net weight must be in units of the International System.
The net weight must be declared as follows:
i. Volume, for liquid foods
ii. Weight, for solid foods
iii. Weight, for semi-solid and viscous foods
In foods preserved in a liquid environment, in addition to the net weight, the drained weight
must also be declared. Liquid environment will be understood as: water, sugar or salty water
based solutions, fruit and vegetable juices and vegetables preserved in vinegar.
4. Name and Address
The name and address of the producer, wholesaler, importer, exporter or retailer must be
written on the label.
5. Industrial and Sanitary Registration
(See Appendix IV)
6. Country of Origin
The country of origin must be printed on the label. When a product's nature is changed in a
second country because of any process change, the second country must be reported as the
country of origin.
7. Lot Identification
Each container must have a clear and distinct identification specifying the manufacturing
company and a lot number.
8. Date and Preserving Instructions
Unless the Codex, or one individual national norm specifies it, the date declaration should
include:
1) The "best before" date (minimum duration date) should be used.
2) This date must have at least the following:
Month and day for products with a minimum shelf life of less than three months.
Month and year for products with a minimum duration of more than three months. If the
month is December use only the year.
3) The date declaration must have the words "Best if consumed before...", for cases other than
the ones in 2.
4) The sentence must be accompanied by:
The date itself.
A reference to the place where the date is printed.
The day, month and year must be numbers not code. The month can be abbreviated using
letters in countries where this practice does not confuse the consumers.
As an exception to 4.7.1 (I) the following products will not need the minimum duration date.
These are:
Fresh fruits and vegetables, including fresh potatoes (not peeled or cut);
Wine, sparkling wines, fruit wines and sparkling fruit wines; Alcoholic beverages with more than
10 percent of alcohol by volume; Bakery products that must be consumed within 24 hours;
Vinegar; Salt (for food); Solid sugar; Candy products; Bubble gum; Specific products, as
determined by the Products Committees, national or Codex; Any special instructions in order to
preserve the product until that date must be printed on the label.
9. User Instructions
Instructions on how to use the product must be printed on the label (especially if the product
needs to be reconstituted).
10. Additional Requirements
a. Quantitative Labeling of the Ingredients
When an important ingredient is printed on the label, the percentage of this ingredient used in
the elaboration of the product (wt./wt.) must be indicated. In addition, when the label
indicates that a product has a low level of an ingredient, the percentage of this ingredient in the
final product must be indicated. Also, it should include the percentage ingredients in the final
product.
If the product name refers to an ingredient, this will not indicate (by itself) that the ingredient
has special importance. This also applies for ingredients such as aromas (or used in small
quantities) on the product label.
b. Exemptions to the Mandatory Labeling Requirements
Except for spices and aromatic herbs, units of product smaller than ten square centimeters
(their largest surface) are exempted of the labeling requirements specified by the previous
sections.
c. Optional Labeling
The labeling of products can have any desired information, as long as it does not violate the
obligatory requisitions of this standard, including the requisitions regarding declaration of
properties and fraud, as of Section 3 (General Principles).
d. Quality Designations
When quality designations are used, they must be easily understandable and not deceptive in
any way.
The data on the label must be clear, so that consumers will be able to read all the information
printed.
When a container is wrapped, the wrapping must have all the required information, or the
container's label must be readable through the wrapping.
The food's name and net weight must be placed in a prominent place and at the same level.
All labels must be in Spanish. For cases when the label is not in this language, a
complementary label containing the information translated into Spanish must be added.
When a new label (or a complementary label) is added to the container, the obligatory
information must reflect the information printed on the original label.