Capitulo III Prod Alimenticiosactualiz 2023-05 1.es - en
Capitulo III Prod Alimenticiosactualiz 2023-05 1.es - en
com
CHAPTER III
OF FOOD PRODUCTS
GENERAL CONDITIONS
Article 155
Both the raw materials, the food additives, as well as the processed products, must respond, in their
chemical composition, appearance, presentation, quality, state of conservation and organoleptic
characteristics, to the specially accepted legal or commercial names.
The preparation, fractioning, possession, circulation, distribution, import, export and delivery to the
consumer of illegal products is prohibited.
The authorization holder and his Technical Director, if applicable, will be personally responsible for the
suitability and identity of the products.
Article 155 bis – (Joint Resolution SPRyRS No. 14/05 and SAGPyA No. 141/05) “Foods of animal origin
(meat and by-products, milk, eggs and honey) must meet the following requirement:
Article 155 tris – (Joint SAGyP and SCS Resolution No. 16/2023)
[As of May 20, 2023, companies are granted a period of two (2) years to adapt their foods to the
established limit of two percent (2%) of trans fatty acids, three (3) years for the adaptation of
ingredients and raw materials to the established limit of two percent (2%) of trans fatty acids and
four (4) years for the elimination of the use of partially hydrogenated oils and fats in the food
industry].
“The content of industrially produced trans fatty acids in foods, including those used as ingredients and
raw materials, should not be greater than 2% of total fat. These limits do not apply to fats from
ruminants, including dairy fat. The use of partially hydrogenated oils and fats in the production of foods,
ingredients and raw materials is prohibited.”
SEEN: The Treaty of Asunción, the Ouro Preto Protocol and Resolutions No. 102/94, 103/94, 35/96, 45/96,
38/98 and 56/02 of the Common Market Group.
CONSIDERING:
That it is necessary to update the Maximum Limits for Inorganic Contaminants in Foods;
That for the purposes of protecting public health it is essential to maintain the content of contaminants at
acceptable toxicological levels;
That the maximum content should be established at the strict level that can reasonably be achieved if
good practices are applied and taking into account the risk related to the consumption of the food;
That the harmonization of the Technical Regulations tends to eliminate the obstacles that are generated
by differences in the current National Regulations, complying with the provisions of the Treaty of
Asunción;
Art. 1 - Approve the “MERCOSUR Technical Regulation on Maximum Limits of Inorganic Contaminants in
Foods”, which appears as an Annex and is part of this Resolution.
Art. 4 - The national organizations competent for the implementation of this Resolution are:
Art. 5 - This Resolution will apply in the territory of the States Parties, to trade between them and to extra-
zone imports.
Art. 6 - This Resolution must be incorporated into the legal system of the States Parties before 1/01/2012.
EXHIBIT
PART I
1- General Criteria:
1.1 - In the foods contemplated in this Regulation, the presence of metallic and non-metallic elements is
allowed, within the established limits, as indicated in Part II.
1.2 - This Technical Regulation does not apply to foods for infants and young children, which will be
governed by the specific Technical Regulations.
1.3 - The levels of inorganic contaminants in foods must be as low as possible, and contamination of the
food at the source must be prevented, the most appropriate technology must be applied in production,
handling, storage, processing and packaging, in order to prevent a contaminated food is marketed or
consumed.
1.4 - Each State Party may establish maximum limits when a MERCOSUR limit has not been agreed upon,
based on the risk analysis for the specific situation, based on the evaluation of scientific data.
1.5 - The maximum permitted contents specified in Part II shall apply to the edible part of the food
products concerned, unless otherwise specifically specified.
1.6 - The maximum contents apply to the product in the state in which it is offered to the consumer.
For products not included in the table in Part II, made from ingredients with limits established in this
Regulation and that have been dried, diluted, transformed or composed of one or more ingredients, the
maximum permitted contents must be deducted from the specific concentration and dilution factors, in
relation to the limits established for the ingredients, which must be provided at the time the competent
Health Authority requests it.
When applying the maximum limits established in Part II to food products that are dried, diluted,
processed or composed of one or more ingredients, the following should be taken into account:
a) changes in the concentration of the contaminant caused by the drying or dilution processes;
If the manufacturer of the product does not communicate the necessary concentration or dilution factor,
or if the competent Health Authority considers that this factor is inadequate, taking into account the
justification communicated, said Authority will define such factor based on the available information.
1.8 - Criteria 1.6 and 1.7 will apply whenever specific maximum contents have not been established for
these dried, diluted, processed or compound food products.
1.9 - Food products that do not comply with the maximum contents established in the attached tables will
not be used as food ingredients.
2 - Specific criteria
2.1 - The maximum content is applied after washing the fruits or vegetables and separating the edible
part accordingly. In the case of potatoes, the maximum content applies to peeled potatoes.
2.2 - The maximum content refers to the edible part of the dried fruits.
2.3 - In the case of cereals, the maximum content applies to:
- unprocessed cereals intended for human consumption;
- cereals intended for direct human consumption, hulled, polished and/or processed when appropriate;
2.5 - Frozen products, pulps and purees of fruits and vegetables, without diluting or concentrating, must
comply with the same limits as vegetables.in nature.
2.6 - The categories of vegetables for the purposes of this Regulation are defined in Part
III.
2.7 - The maximum limits are expressed in milligrams per kilogram (mg/kg), except in the case of wine
which is expressed in milligrams per liter (mg/L).
2.8 - In the case of liquid products, the maximum limits can be expressed in mg/L, as long as their density
does not differ by more or less 5% in relation to the density of water.
PART II
ARSENIC
Sugars 0.10
Honey 0.30
Hard and soft candies and similar including chewing gum 0.10
cocoa paste 0.50
Chocolates and cocoa products with less than 40% cocoa 0.20
Chocolates and cocoa-based products with more than 40% cocoa 0.40
Non-alcoholic drinks (excluding juices) 0.05
Juices and fruit nectars 0.10
Fermented and ferment-distilled alcoholic beverages, except wine 0.10
Came 0.20 mg/L
Sugars 0.10
Honey 0.30
Hard and soft candies and similar including chewing gum 0.10
cocoa paste 0.50
Chocolates and cocoa products with less than 40% cocoa 0.20
Chocolates and cocoa-based products with more than 40% cocoa 0.40
Non-alcoholic drinks (excluding juices) 0.05
Juices and fruit nectars 0.05
Fermented and ferment-distilled alcoholic beverages, except wine 0.20
Came 0.15mg/L
Honey 0.10
cocoa paste 0.30
Chocolates and cocoa products with less than 40% cocoa 0.20
Chocolates and cocoa-based products with more than 40% cocoa 0.30
Non-alcoholic drinks (excluding juices) 0.02
Juices and fruit nectars 0.05
Fermented and ferment-distilled alcoholic beverages, except wine 0.02
Fluid milk ready for consumption and dairy products without addition, without 0.05
dilute or concentrate
Cheeses 0.50
Bovine, ovine, pork, goat and poultry meat, raw, frozen or chilled 0.05
derivatives, sausages and breaded meats
raw
Crustaceans 0.50
MERCURY
TIN
PART III
a) Inflorescences
- Cauliflower (Pella),Brassica oleraceaL. subvar.cauliflora(Garsault) DC.
- Broccoli (green or violet Pella),
- Italian:Brassica oleraceavar.italicPlenck.
- Head or French:Brassica oleraceaL. subvar.cymosaDuchesne.
-Grelo,Brassica napusL.
- Others.
c) Fleshy stem:
- Cabbage-radish: white or violet stemBrassica oleraceaL. var.gongyloidesL.
II. Leafy vegetables (includingBrassicasloose leaves) and fresh aromatic herbs This category includes the
following species:
c) Vine leaves
- Vitis viniferaL.
d) Watercress
- Watercress,Rorippa nasturtium-aquaticum(L.) Hayek.
e) Endives
- Endive or endive,Cichorium endiviaL.
f) Aromatic herbs
- Basil,Ocimum basilicumL.
- Chives or chives,Allium fistulosumL. andAllium schoenoprasumL.
- Tarragon, estragonium, tarragón or dragoncillo,Artemisia dracunculusL.
-Laurel,Laurus nobilisL.
- Oregano,Origanum vulgareL.
- Parsley,Petroselinum crispumMill. Fuss.
- Rosemary,Rosmarinus officinalisL.
- Sage,Salvia officinalisL.
- Thyme,Thymus vulgarisL.
- Others.
- Garlic,Allium sativumL.
- Onion,Allium cepaL.
- Green onion,Allium cepaL.
- Shallot,Allium escalonicumL.
- Others.
IV. family fruit vegetablesCucurbitaceae This category
includes the following species:
- Others.
a) Solanaceae:
- Eggplant,Solanum melongenaL.
- Gombo, okra, okra, Turkish chili or Turkish chaucha,Abelmoschus esculentus(L.) Moench.
- Pepper,Capsicum annuumL.
- Tomatoes,Lycopersicon esculentumMill.
- Others.
b) Corn:
- Choclo or sweet corn,Zea maysL. var. saccharata (Sturtev.) LH Bailey.
- Others.
VIII. Mushrooms
This category includes the following genres:
a) Potato or Potato:
- Potato or potato,Solanum tuberosumL.
- indigenous potato,Solanum tuberosumL. subsp.andigena(Judge & Bukasov) Hawkes and other
species ofSolanumSect.Tuberarium(Dunal) Bitter
All legislation of the Argentine Food Code that opposes the issuance of this Resolution is repealed.
1 reach
1.1. Aim
This Regulation establishes the maximum permissible limits of aflatoxins in fluid milk, powdered milk,
peanuts, peanut paste, corn grains and corn flour or semolina for human consumption, as well as the
corresponding sampling plans and methods of analysis. 1.2. Area of application
This Regulation applies to fluid milk, powdered milk, peanuts, peanut paste, corn grains and corn flour or
semolina marketed in the territory of the States Parties, including extra-zone imports.
2. References
2.1 "Sampling plans for aflatoxin analysis in peanuts and corn", FAO Food and Nutrition Paper 55, 1993.
2.2 Association of Official Analytical Chemists. 1990 "Official Methods of Analysis of the Association of
Official Analytical Chemists" 15th ed.
2.3 FIL-IDF Standard 50 B 1985 "Sampling methods for milk and milk products".
2.4 Standard ISO 950: 1979 "Cereal - Sampling (as grain)".
2.5 Waltking, A.E. 1980. "Sampling and Preparation of Samples of Peanut Butter for Aflatoxin Analysis." J.
Assoc. Off. Anal. Chem. 63: 103 - 106.
3. Requirements
MAXIMUM PERMISSIBLE LIMITS OF AFLATOXIN CONCENTRATION
4. Sampling Methods
4. 1. Milk
For the collection of samples of powdered milk and fluid milk, the FIL-IDF 50 B: 1985 standard "Sampling
methods for milk and milk products" and/or its updates will be used. Samples of fluid or powdered milk
will be subdivided into a minimum of three subsamples. Subsamples of fluid milk will be kept frozen;
Subsamples of milk powder will be stored in non-permeable containers, at a maximum relative humidity
of 60% and a maximum temperature of 25° C. The size of the aliquot of milk powder for analysis will be 25
g (instead of the 5 g indicated in the AOAC procedure 980.21, 1990) which will be dissolved in 250 ml and
homogenized; An aliquot of 50 ml will be taken from this suspension and continued as indicated in the
aforementioned procedure.
The laboratory peanut sample (5 kg) will be transformed into a homogeneous paste or ground to 14
mesh, in its entirety, homogenized and subsequently divided into a minimum of three parts. A fourth
subsample may be taken for routine analysis. The samples and subsamples of peanuts and corn collected
will be stored in paper containers,
cotton or other material at a maximum relative humidity of 60% and a maximum temperature of 25° C.
4.3. Cornmeal
For packaged product: One sample will be made per batch of 50 tons or less. A number of units will be
collected at random equal to the square root of the number of packages that make up the lot or 1% (one
percent) of them, whichever is smaller. When the number of units calculated is fractional, the higher
whole number will be taken. A minimum of 50 g will be extracted from each of the units. These aliquots
will be homogenized and at least 300 g will be divided into three subsamples. A fourth subsample may be
taken for routine analysis.
For bulk product: The procedure will be as indicated in paragraph 4.2. for bulk corn. 4.4. Peanut Paste
(peanut paste or peanut butter)
The sampling procedure described in reference (2.5) will be used.
5. Analysis Methods
5.1. Reference Analysis Methods
5.1.1. Milk.- For the determination of aflatoxin M1 in fluid milk and powdered milk, the AOAC 980.21
procedure, published in reference (2.2) and/or its respective updates, will be used. The control of
standard solutions will be carried out according to the AOAC procedure 970.44 and 971.22, of the same
publication.
5.1.2. Corn.- For the determination of total aflatoxins (B1+B2+G1+G2) in corn and in corn flour or
semolina, the AOAC 968.22 procedure will be used, cited in reference (2.2) and/or its respective updates.
The control of standard solutions will be carried out according to the AOAC procedure 970.44 and 971.22,
of the same publication.
5.1.3. Peanuts.- For the determination of total aflatoxins (B1+B2+G1+G2) in peanuts and peanut paste, the
AOAC 970.45 procedure published in reference (2.2) and/or its respective updates will be used. The
control of standard solutions will be carried out according to the AOAC procedure 970.44 and 971.22, of
the same publication.
5.2. Routine Analysis Methods.- For the determination of aflatoxins in fluid milk and powdered milk, corn,
corn flour, peanuts and peanut paste, the usual routine procedures in each country, which are
internationally validated, will be used.
6.3. In the event that the lot is rejected in the first analysis, at the request of the interested party, the
laboratory that carried out the first analysis will carry out the analysis on the second subsample, in the
presence of the technical experts indicated by the interested parties.
6.4. In the event of a discrepancy between the analytical results of the first and second subsample, the
analysis of the third subsample may be carried out by the same laboratory, with its result being final.
6.5. In the analysis of the second and third subsample, the same batch acceptance or rejection criteria
established in sections 6.1 and 6.2 of this Resolution will be adopted.
GMC RESOLUTION Nº 059/93
Incorporated by Resolution MSyAS No. 003 of 01/11/95
All legislation of the Argentine Food Code that opposes this Resolution is repealed.
Art 2.- The State Parties will put into effect the legislative, regulatory and administrative provisions
necessary to comply with this Resolution and will communicate the text of the same to the Common
Market Group, through the Administrative Secretariat.
Art 3.- This Resolution will come into force as of December 31, 1993.
APPENDIX 1
Introduction
The general principles to be applied to establish microbiological criteria and standards for foods are
justified by public health problems and the need to standardize standards for trade between countries.
For this reason, international organizations such as FAO, WHO, PAHO, have shown growing concern on
the issue.
Thus, the CODEX ALIMENTARIUS and the ICMSF have continually published normative documentation
that regulates the subject.
Considering that the countries that make up MERCOSUR integrate and actively participate in the
preparation of the CODEX ALIMENTARIUS and ICMSF documents, the latter may be taken as a reference.
CRITERIA AND PATTERNS APPLICABLE TO FOOD MICROBIOLOGY. General principles for its
establishment
Considerations on the principles for the establishment and application of Microbiological Standards and
Standards.
1.- The principles are those indicated in the documents prepared by the CODEX ALIMENTARIUS.
These principles must respect provisions established in documents that deal with Good Manufacturing
Practices and their forms of evaluation, such as Risk Analysis and Critical Point Control.
2.- In situations of epidemiological risk that justify a Health Alert, other microbiological determinations
not included in the established Standards and Standards must be carried out, depending on the problem.
Creams
Butter, etc.
Meat products that are consumed without heat treatment:
Sausages
Sausages
Cold cuts
Salty
Smoked, etc.
Refrigerated foods:
Birds
Vegetables
Fish and shellfish, etc. Frozen
food:
Ready meals
Ice creams
Fish and seafood
Vegetables
Ice, etc.
Fresh pasta (with and without filling)
Non-alcoholic drinks:
Water
Fruit juices, etc. Condiments:
sauces and dressings Dried fruits:
peanuts, etc.
Canned plant and animal products Other foods
deemed necessary
Analytical Determinations
The criteria established by CODEX ALIMENTARIUS ICMSF and other internationally recognized
organizations will be taken as a reference.
Article 156 tris – (Joint Resolution SPReI and SAV No. 4 - E/2017)
[As of January 10, 2017, companies are given a period of one hundred eighty (180) business days to
adapt]
“Prepared food ready for consumption is understood to mean the culinary preparation resulting from the
preparation, with or without cooking, of one or more food products of animal or plant origin, with or
without the addition of other substances authorized for consumption.
It may be packaged or divided whether or not it is visible to the consumer at the time of dispensing, and
be ready for consumption directly or after heating.
All foods contemplated in other categories of this Code are excluded from this definition.
The following criteria will be applied to food that is dispensed in establishments with or without kitchen
such as restaurants, school cafeterias, companies, hospitals, residences, means of transportation, among
others, as well as to food produced by establishments that are dedicated to the preparation of prepared
meals, which are marketed for consumption inside or outside such as central kitchens, and retail take-
away establishments.
II. Meals prepared with heat treatment that subsequently include ingredients not subjected to heat
treatment.
III. Foods prepared with heat treatment that receive a post-heat treatment handling process such as
cutting, mixing, slicing, packaging, among others.
IV. Prepared meals that, at the end of their preparation, have been subjected as a whole to a thermal
process.
Meals prepared ready for consumption must meet the following microbiological specifications: for those
prepared according to items I, II and III, table 1 corresponds and for those prepared according to item IV,
table 2 corresponds.
In situations of epidemiological risk that justify a health alert, other microbiological determinations may
be carried out, depending on the problem.
Table 1
Parameter Acceptance requirements Methodology(1)
Count
ISO 21528- 2:2004
Enterobacteriaceae(2) n=5, c=2, m=103, M=104
ICMSF
(CFU/g)
ISO 16649-3:2005
CountE.coli
n=5, c=0, m<3 ICMSF (method 1)
(NMP/g)
BAM-FDA:2002 (method 1)
Coagulase-positive ESO 6888-3:1999
n=5, c=1, m=102, M=103
Staphylococcus count (MPN/g) ICMSF
ISO 6579:2002,
Salmonellaspp. n=5, c=0, Absence in 25 g Co: 2004
BAM-FDA:2011
USDA-FSIS:2011
ISO 11290-1:1996,
Listeria
n=5, c=0, Absence in 25 g AMD:2004
monocytogenes
BAM-FDA:2011
USDA-FSIS:2009
CountClostridium
n=5, c=1, m=102, M=103 ISO 7937:2004
perfringens(3)(CFU/g)
Count of suspects
n=5, c=1, m=102, M=103 ISO 7932:2004
Bacillus cereus(4)(CFU/g)
USDA-FSIS:2010
E.coliO157:H7/NM(5) n=5, c=0, Absence in 65 g ISO 16654:2001
BAM-FDA:2011
ISO 13136:2012
E.colinot O157(5) (6) n=5, c=0, Absence in 65g
BAM-FDA:2014
(1)or its most updated version.
(2)Ifraw vegetable ingredients are used, do not make this determination.
(3)Include only in foods with meat.
(6)E.coliShiga toxin producer of serogroups: O145, O121, O26, O111 and O103. Only isolates positive for
Table 2
Parameter Acceptance requirements Methodology(1)
Aerobic count
ESO 4833:2003
mesophiles n=5, c=2, m=104, M=105
BAM-FDA:2001
(CFU/g)
Enterobacteriaceae count ESO 21528-2:2004
n=5, c=2, m=102, M=5.102
(CFU/g) ICMSF
ISO 16649-3:2005
CountE.coli
n=5, c=0, m<3 ICMSF (method 1)
(NMP/g)
BAM-FDA:2002 (method 1)
Coagulase-positive ISO 6888-3:1999
n=5, c=1, m=10, M=102
Staphylococcus count (MPN/g) ICMSF
ISO 6579:2002,
Salmonellaspp. n=5, c=0, Absence in 25 g
Co: 2004
BAM-FDA:2011
USDA-FSIS:2011
ISO 11290-1:1996,
Listeria
n=5, c=0, Absence in 25 g AMD:2004
monocytogenes
BAM-FDA:2011
USDA-FSIS:2009
Count of suspects
n=5, c=1, m=102, M=103 ISO 7932:2004
Bacillus cereus(2)(CFU/g)
CountClostridium
n=5, c=1, m=102, M=103 ISO 7937:2004
perfringens(3)(CFU/g)
USDA-FSIS:2010
E.coliO157:H7/NM(4) n=5, c=0, Absence in 65 g ISO 16654:2001
BAM-FDA:2011
ISO 13136:2012
E.colinot O157(5) (6) n=5, c=0, Absence in 65g
BAM-FDA: 2014
(1)or its most updated version
(2)Include only in foods with cereals, potatoes, starchy foods
(3)Include only in foods with meat
(4)Include only in foods prepared with minced meat, such as meatballs, empanadas, cakes, rolls or similar.
Sampling of these food products will be carried out, whenever possible, in accordance with the sampling
plans established in this article.
When the total number of units in the lot is equal to or less than 100 units, an indicative sample will be
taken (n = 1).
- for parameters that present a 2-class sampling plan, maintain the plan and the sample aliquot analyzed
in grams for each parameter; that is, acceptance or rejection, depending on the presence or absence of
the microorganism investigated in the indicative sample.
- for parameters that present a 3-class plan, move to a 2-class plan where no value should exceed the
proposed M, that is, acceptance if the count of the microorganism in the indicative sample is ≤ M and
rejection if the count of the microorganism in the indicative sample is > M.
The result of the indicative sample is interpreted for the entire lot or batch.”
Art 2.- The States Parties will put into effect the legislative, regulatory and administrative provisions
necessary for compliance with this Resolution through the following organizations:
Argentina: Ministry of Health; National Administration of Drugs, Foods and Medical Technology.; National
Food Institute. Ministry of Economy. Ministry of Agriculture, Livestock, Fisheries and Food. National Agri-
Food Health and Quality Service.
Uruguay: Ministry of Public Health. Ministry of Industry, Energy and Mining. Technological Laboratory of
Uruguay.
Art 3.- This Resolution will apply in the territory of the States Parties, to trade between them and to extra-
zone imports.
Art 4.- The States Parties of MERCOSUR must incorporate this Resolution into their national legal systems
before 1/1/2001.
XXXIX GMC- Brasilia, 29/IX/00
EXHIBIT
In addition to the additives listed below, additives that come from the ingredients used may be
present, according to the principle of additive transfer.
ACIDULANT
All those authorized as GMP in MERCOSUR quantum satis
334 Tartaric acid 0.025
338 Phosphoric Acid, Ortho-Phosphoric Acid 0.50
FIRMNESS AGENT
All those authorized as GMP in MERCOSUR quantum satis
ANTI-FOAMING
All those authorized as GMP in MERCOSUR quantum satis
900 Dimethylpolysiloxane 0.001
ANTIOXIDANT
All those authorized as GMP in MERCOSUR quantum satis
220 Sulfur Dioxide, Sulfurous Anhydride 0.02
221 Sodium Sulfite 0.02 (as SO2)
222 Sodium Bisulfite, Sodium Acid Sulfite 0.02 (as SO2)
223 Sodium Metabisulfite 0.02 (as SO2)
224 Potassium Metabisulfite 0.02 (as SO2)
225 Potassium Sulfite 0.02 (as SO2)
226 Calcium Sulfite 0.02 (as SO2)
227 Calcium Bisulfite, Calcium Acid Sulfite 0.02 (as SO2)
228 Potassium Bisulfite 0.02 (as SO2)
306 Tocopherols: concentrated mixture 0.03 on fat matter
307 Tocopherol: Alpha-Tocopherol 0.03 on fat matter
310 Propyl Galate 0.02 on fat matter
319 Tert-Butyl Hydroxyquinone, TBHQ, Tertiary 0.02 on fat matter
Butylhydroquinone
320 Butyl Hydroxyanisole, BHA, Butylated Hydroxyanisole 0.02 on fat matter
321 Butylated Hydroxytoluene, BHT,Butylated Hydroxytoluene 0.01 on fat matter
FLAVORING/FLAVORING
All those authorized in MERCOSUR quantum satis
COLORANT
100i Turmeric, Curcumin 0.005 (as curcumin)
101i Riboflavin quantum satis
101ii Riboflavin 5'- Sodium Phosphate quantum satis
102 Tartrazine 0.005
110 Sunset Yellow FCF, Sunset Yellow 0.005
120 Cochineal, Carminic Acid, Carmine 0.005
122 Azorubine 0.005
124 Ponceau 4R, Cochineal Red A 0.005
129 Red 40, Red Allura AC 0.005
131 Patent Blue V 0.005
132 Indigotin, Indigo Carmine 0.005
133 Bright Blue FCF 0.005
140i Chlorophyll quantum satis
140ii Chlorophyllin quantum satis
141i Cupric Chlorophyll 0.040
141ii Cupric Chlorophyllin, sodium and potassium salts 0.040
150th Candy I – Simple quantum satis
150b Caramel II - Caustic Sulphite Process quantum satis
150c Candy III - Ammonium Process quantum satis
150d Caramel IV - Ammonium Sulfite Process quantum satis
153 Charcoal quantum satis
160a i Beta-Carotene (Synthetic Identical to natural) 0.020
160a ii Carotenes: Natural Extracts 0.020
160b Rocu/ Annatto/ Urucu/ Bixin/ Norbixin 0.015 (as bixin)
160c Paprika/Capsanthin/Capsorubin quantum satis
160d Lycopene 0.005
160e Beta-Apo-8'Carotenal 0.020
160f Methyl or Ethyl Ester of Beta-Apo-8'-Carotenoic Acid 0.020
CONSERVATIVE
(except for frozen products)
All those authorized as GMP in MERCOSUR quantum satis
200 Sorbic acid 0.10
201 Sodium Sorbate 0.10 (as sorbic acid)
202 Potassium Sorbate 0.10 (as sorbic acid)
203 Calcium Sorbate 0.10 (as sorbic acid)
THICKENER
All those authorized as GMP in MERCOSUR quantum satis
STABILIZER
All those authorized as GMP in MERCOSUR quantum satis
339ii Sodium-(di)Phosphate, Sodium-(di)Monophosphate, Sodium- 0.30 (as P2EITHER5)
(di)Orthophosphate
432 Polyoxyethylene (20) Sorbitan Monolaurate 0.10
433 Polyoxyethylene (20) Sorbitan Monooleate 0.10
434 Polyoxyethylene (20) Sorbitan Monopalmitate 0.10
435 Polyoxyethylene (20) Sorbitan Monostearate 0.10
436 Polyoxyethylene (20) Sorbitan Tristearate 0.10
450i Sodium-(di)Diphosphate, Sodium Diphosphate 0.30 (as P2EITHER5)
450ii Sodium-(tri)Diphosphate 0.30 (as P2EITHER5)
450iii Sodium-(tetra) Diphosphate, Sodium Pyrophosphate 0.30 (as P2EITHER5)
450v Potassium-(tetra) Diphosphate, Neutral Potassium Pyrophosphate 0.30 (as P2EITHER5)
450vii Calcium-(mono) Diphosphate, Calcium Biphosphate, Calcium 0.30 (as P2EITHER5)
Diphosphate Diacid
451i Sodium-(penta)Triphosphate, Sodium Tripolyphosphate 0.30 (as P2EITHER5)
451ii Potassium-(penta) Triphosphate, Potassium Tripolyphosphate 0.30 (as P2EITHER5)
452i Sodium polyphosphate, Sodium metaphosphate, Sodium 0.30 (as P2EITHER5)
Hexametaphosphate
452ii Potassium Polyphosphate, Potassium Metaphosphate 0.30 (as P2EITHER5)
452iii Calcium and Sodium Polyphosphate 0.30 (as P2EITHER5)
473 Esters of Fatty Acids with Sucrose, Fatty Esters of Sucrose, 0.20
Saccharoesters
474ii Glycerol and Sucrose Esters, Sucroglycerides 0.20
GELIFYING
All those authorized as GMP in MERCOSUR quantum satis
FLAVOR HIGHLIGHTER
All those authorized as GMP in MERCOSUR quantum satis
ACIDITY REGULATOR
All those authorized as GMP in MERCOSUR quantum satis
450i Sodium-(di)Diphosphate, Sodium Diphosphate 0.30 (as P2EITHER5)
450ii Sodium-(tri)Diphosphate 0.30 (as P2EITHER5)
450iii Sodium-(tetra) Diphosphate, Sodium Pyrophosphate 0.30 (as P2EITHER5)
450v Potassium-(tetra) Diphosphate, Neutral Potassium Pyrophosphate 0.30 (as P2EITHER5)
450vii Calcium-(mono)Diphosphate, Calcium Biphosphate, Calcium 0.30 (as P2EITHER5)
Diacid Diphosphate
451i Sodium-(penta)Triphosphate, Sodium Tripolyphosphate 0.30 (as P2EITHER5)
451ii Potassium-(penta) Triphosphate, Potassium Tripolyphosphate 0.30 (as P2EITHER5)
KIDNAPPER
All those authorized as GMP in MERCOSUR quantum satis
385 Sodium-(di) EDTA Calcic, Calcium disodium 0.01
Ethylenediamine Tetraacetate
386 Sodium-(di) EDTA, Sodium-(di) Ethylenediamine 0.01
Tetraacetate
21.2. DEHYDRATED
Dehydrated Industrial Culinary Preparations, based on ingredients of plant and/or animal origin,
processed or not, not included in other categories
The same functions are allowed as for Industrial Culinary Preparations Ready for Consumption, except
Preservatives and additives for each function in quantities such that the product ready for
consumption contains a maximum of the concentration established for the subcategory Industrial
Culinary Preparations Ready for Consumption. The use of Antihumectants / Anti-caking Agents and
Humectants is also permitted, as indicated below.
ANTIHUMECTANT
All those authorized as GMP in MERCOSUR quantum satis
341iii Calcium-(tri) Phosphate, Calcium Tribasic Phosphate, Calcium-(tri) 1.0 (as P2EITHER5)
Orthophosphate
MOISTURIZER
All those authorized as GMP in MERCOSUR
Article 156 quater – Joint Resolution SRYGS and SAB Nº22/2019.
[As of July 23, 2019, companies are given a period of twenty-four (24) months to adapt]
Level
Part of the product
Maximum
Analyte basic/product to which the Sampling Plan(*)
(NM)
maximum level (ML) applies
(ug/kg)
Cereal-based foods for infants and young children(**)
Deoxynivalenol 200 CODEX-STAN
According to
The ML is applied to products on a
193-1995, last
Ochratoxin A 0.5 dry matter basis.
modification(***)
Corn flour and corn grits
According to CODEX-STAN
Deoxynivalenol 1000 All product 193-1995, last
modification(***)
According to CODEX-STAN
Fumonisins
2000 All product 193-1995, last
(B1+B2)
modification(***)
According to Regulation
Ochratoxin A 3 All product
(EC) No 401/2006, EU
Flour, semolina, semolina, and wheat flakes
According to CODEX-STAN
Deoxynivalenol 1000 All product 193-1995, last
modification(***)
According to Regulation
Ochratoxin A 3 All product
(EC) No 401/2006, EU
Coffee
Soluble Coffee (Instant)
According to Regulation
Ochratoxin A 10 All product
(EC) No 401/2006, EU
Roasted coffee beans and ground roasted coffee, excluding soluble coffee
According to Regulation
Ochratoxin A 5 All product
(EC) No 401/2006, EU
Raisins (currants, sultanas and other varieties of raisins)
According to Regulation
Ochratoxin A 10 All product
(EC) No 401/2006, EU
(*) Sampling of food products prepared for sale to the public must be carried out, whenever possible, in
accordance with sampling plans described for each case. When this is not possible, the Sampling Plans
described in article 1416 of this Code - Sampling Systems - may be applied, provided that said method
guarantees that the sample is representative of the lot being sampled.
In both cases, the sample size should not be less than 1kg.
(**) Young children are understood to be children over twelve months and up to three years (Codex Stan
73-1981 Latest Amendment 2017).
(***) Last amendment 2017.
Article 156 fifth (SCS and SAByDR Joint Resolution No. 09/2021)
[As of February 2, 2021, companies are given a period of twenty-four (24) months to adapt]
Part of Product
basic / Part of the Product
Level maximum
Analyte that HE Sampling Plan
(NM) (ug/kg)
apply he level
maximum (NM)
HEgun Regulation
Patulin 10 All product(#)
(EC) No 401/2006, EU
According to Regulation
Aflatoxin M1 0.025 All product(#)
(EC) No 401/2006, EU
Breakfast cereals
According to Regulation
Deoxynivalenol 500 All product
(EC) No 401/2006, EU
According to Regulation
Zearalenone(TO) fifty All product
(EC) No 401/2006, EU
(##) Also applies to Foods for Specific Medical Purposes intended for infants or young children.
CONSERVATION AND TREATMENT OF PRESERVED OR PRESERVED
FOOD
Article 157
Perishable foods are understood to be those that, due to their composition and/or physicochemical and
biological characteristics, may experience alterations of various nature that reduce or nullify their
acceptability in variable periods of time.
They require special conservation, storage and transportation conditions.
(Res MSyAS 25 of 08/14/95) "All interjurisdictional transport of perishable foods due to their
characteristics must carry thermographic equipment to control and record temperatures, in order to
verify the correct cold chain from its origin to place of destination, when the distance to be traveled
exceeds 70 (seventy) km. These thermographs will be sealed from the origin and may be controlled by the
jurisdictional health authorities. The jurisdictional Health Authority within its territory may require and
verify the use of the thermograph." .
Article 158
Preserved Foods or Preserved Foods are understood to be those that, having been subjected to
appropriate conservation or preservation treatments, are maintained in the proper hygienic-sanitary
conditions and acceptability for consumption for variable periods of time.
2. Be frozen, packaged and marketed in accordance with the technological requirements established in
Article 162 of this Code."
Article 160
Cold preservation (refrigeration or freezing) is understood as subjecting food to the action of low
temperatures to fundamentally inhibit or eliminate microbial and enzymatic activities. In these
treatments, the temperature, relative humidity and air circulation required by each food will be taken into
account.
Article 161
Refrigeration is understood as subjecting food to the action of low temperatures without reaching
freezing temperatures.
Refrigeration temperatures will remain uniform and without sudden changes during the conservation
period and will be appropriate for each type of product.
Freezing temperatures throughout the storage period will remain uniform and appropriate for each type
of product.
The Slow Freeze and Fast Freeze designations are linked to the freezing rates, according to the
procedures used.
Food that is frozen must be presented in perfect hygienic-sanitary conditions.
Its initial microbial content, prior to being subjected to the conservation process, must ensure the
stability of the product until the moment of consumption.
Defrosting is understood as conveniently tempering the frozen product until its temperature is at all
points higher than its freezing point.
When it is carried out industrially, it will be carried out under the appropriate conditions for each type of
product.
Food may not be subjected to successive thawing and freezing processes.
Rapid freezing, Superfreezing or Superfreezing is understood as subjecting food (raw materials and/or
processed products) to a sudden cooling process that allows the temperature of maximum crystallization
to be quickly exceeded, in a time that should not exceed 4 hours.
The rapid freezing, superfreezing or superfreezing process may be considered complete when, once
thermal stabilization has been achieved, the entire product (regardless of the measurement point) has a
temperature of -18°C or lower.
Quick-frozen, super-frozen or super-frozen foods must be stored in refrigerated chambers suitable for
maintaining the temperature of the products, practically at constant values and always equal to or lower
than -18°C.
The transportation of these products will be carried out in vehicles provided with the necessary
equipment to maintain the temperature indicated in the previous paragraph, a condition that must also
be met by conservators or refrigerators for sale to the public.
The packaging of these foods must be of a nature that ensures good preservation and inviolability, as
well as resistance to rapid freezing or superfreezing procedures and subsequent culinary heating. The
latter when expressly indicated by the method of preparation.
On the labeling, in addition to the regulatory requirements, the following must be stated:
a) The legend Frozen, Superfrozen or Superfrozen as appropriate, with very notable characters on the
main face of the labeling.
b) The date of preparation (month and year) and the indication of the expiration time in characters of very
good size, prominence and visibility on the main face of the labeling.
c) The instructions for use, clearly specifying the method of defrosting, the precautions to be taken for the
culinary preparation of the product, the conservation until the moment of consumption and the method
of heating."
Article 163
Preservation by heat (sterilization, industrial or technical sterilization, pasteurization) is understood as
subjecting food to the action of adequate temperatures and times to fundamentally eliminate or reduce
microbial and enzymatic activities.
Article 164
Sterilization, without qualification, is understood to be the process that destroys in food, at appropriate
temperatures, all life forms of pathogenic and non-pathogenic microorganisms.
Article 165
Industrial or Technical Sterilization is understood, without any other qualification, as the thermal process
that, applied to food, ensures:
a) Conservation without alteration and good commercial quality for a sufficiently long period, compatible
with commercial needs.
b) Absence of microorganisms harmful to the health of the consumer (pathogenic germs, toxicogenic
germs) and absence of toxins.
c) Absence of any microorganism capable of proliferating in the food, which means the absence of any
alteration of microbial origin.
Article 166
Pasteurization or Pasteurization is understood as subjecting foods to the action of temperatures below
100°C and for sufficient times to destroy the vegetative forms of the common types of pathogenic
microorganisms and a certain proportion of the non-pathogenic ones that contaminate them. so that the
product thus treated can be maintained, transported, distributed, consumed or used in other processes
under conditions of acceptability at appropriate temperatures and for reasonable times according to the
nature of the product.
Article 167
Drying is understood as subjecting food to natural environmental conditions to deprive it of most of the
water it contains.
Article 168
Dehydration is understood as subjecting food to the main action of artificial heat to deprive it of most of
the water it contains.
Article 169
Freeze drying means subjecting food to freezing processes followed by sublimation of the ice formed to
deprive it of most of the water it contains.
Article 170
Salting (dry or brine) is understood as subjecting food to the action of edible salt with or without other
condiments.
Dry Salting is understood as subjecting the external surfaces of foods to contact with salt under
appropriate environmental conditions.
Preservation in Brine is understood as subjecting food to the action of salt solutions in varying
concentrations and times, depending on the nature of the product.
Smoked products must not contain more than 1.0 micrograms per kilogram: (1ppb) of 1,2 benzopyrene,
3,4 benzopyrene, fluorene, phenanthrene, other polycyclic hydrocarbons (isolated or in a mixture) of toxic
or harmful action for the health."
The liquid phase of the pickles after stabilization must have a maximum pH (at 20°C) of 4.5. Those
products with a pH greater than 3.5 and up to 4.5 must be subjected to a heat treatment that ensures the
safety of the final product.
Pickled or pickled products must comply with the labeling standards of this Code.
The temperature and relative humidity conditions of each food during the transportation, irradiation and
storage period must be appropriate for each type of product.
Foods treated with ionizing energy must retain their characteristics as indicated in article 158 of this
Code.
To subject foods to the action of ionizing energy, the following points must be met:
1. Technological requirements:
1.1. Food irradiation is only justified when it responds to a technological need or when it contributes to
achieving a food hygiene objective, and should not be used as a substitute for Good Manufacturing
Practices.
1.2. The doses used must be appropriate to the technological and public health objectives pursued and
conform to appropriate irradiation treatment practices.
1.3. The packaging materials for these foods must meet the requirements of article 184 of this Code and
must be of a nature that ensures good preservation and inviolability, as well as compatible with the
irradiation process. Likewise, the materials of the containers or wrappers must prevent reinfestation with
insects and/or microbial recontamination and have a permeability to oxygen, carbon dioxide and water
vapor that ensures the useful life of the irradiated product.
Purposes:
a) Control of pathogenic microorganisms. 10
b) Disinfestation of insects. 1.0
CLASS 5 – EDIBLE CULTIVATION FUNGI, FRESH
Purposes:
a) Control of spoilage microorganisms 3.0
CLASS 6 – FISH AND SEAFOOD, AND THEIR PRODUCTS (FRESH
AND FROZEN)
Purposes:
a) Control of spoilage and pathogenic microorganisms. 5.0 (**)
b) Parasite control. 2.0 (***)
CLASS 7 – POULTRY, BEEF, PORK, GOAT, OTHERS AND THEIR
PRODUCTS (FRESH AND FROZEN) Purposes:
Purposes:
a) Insect control. 1.0
b) Fungal control. 3.0
(*) The overall average absorbed dose should not be greater than 30 kGy.
(**) The minimum dose is defined based on the hygienic quality of the product. (***) The
minimum dose can be defined based on the type of parasite.
3. Repeated irradiation
Except for foods in classes 3, 4 and 8 that are irradiated for the purpose of controlling reinfestation by
insects, foods should not be subjected to repeated irradiation.
3.2. The accumulated absorbed dose should not be greater than 10kGy as a result of repeated irradiation,
except when this is necessary to achieve a legitimate technological purpose.
Together with the NATIONAL REGISTRY OF FOOD PRODUCERS, the competent authority must keep a
particular registry of industrial irradiation facilities, assigning them a reference number and making all
the corresponding communications and publications.
In all cases, intervention must be given to the ARN and the CNEA to comply with the functions established
in the National Law of Nuclear Activity No. 24,804, Decree No. 1390/98.
Likewise, to control the process within the facility, appropriate records will be kept, particularly those
referring to quantitative dosimetry.
6. Labeling
They must comply with the provisions for labeling packaged foods in current legislation.
6.1. The labeling of irradiated foods and those that contain irradiated components in a proportion that
exceeds 10% of the total weight, and are sold packaged for direct consumption, must be labeled
indicating the legend 'Food treated with ionizing energy' or 'Contains treated components'. with ionizing
energy', respectively, with characters of good size, enhancement and visibility. The logo recommended by
the Codex Alimentarius Food Labeling Committee must also be used.
In the case of irradiated foods that are sold to the final consumer in unpackaged form, the logo and the
phrase 'Food Treated with Ionizing Energy' will be displayed to the consumer either:
7. Post-irradiation verification
When necessary and applicable, analytical methods may be used for the detection of irradiated foods.
The characteristics and requirements will be expressly considered in the particular cases in which this
Code authorizes the procedure."
The use of food additives will be done only in specifically authorized cases, complying with all the
requirements that this Code establishes on the matter."
Article 175
The name "Canned food" refers to products of animal or plant origin that, packaged in an airtight
manner, have been subjected, before or after packaging, to authorized conservation processes.
Article 176
It is prohibited to manufacture preserved foods for sale: 1. In unauthorized
establishments.
2. With substances that are altered, damaged, infected, poorly preserved, lacking nutritional properties or
that for any reason are unsuitable for food.
3. With procedures that do not meet the necessary sanitary conditions or that do not guarantee the good
conservation of the product.
4. Using substances and packaging prohibited by this document and by the health authority.
To judge the degree of corrosion that affects the canned container, the maximum contents of metals and
metalloids established by Article 156 of this Code will be taken into account.
Any preserved food that circulates from a factory not officially authorized or is kept in storage, displayed
or sold, will be confiscated immediately."
COLD ROOMS
Article 178
A cold room is understood to be a closed space intended for the preservation of food by means of
artificial cold.
All food products that are stored in cold rooms are understood to be intended for food and, therefore,
those that are not suitable for consumption will be confiscated immediately.
The cold rooms must be disinfected as many times as necessary and their interior temperature may
under no circumstances be higher than the corresponding temperature according to the nature of the
food being preserved.
They will be kept in perfect conditions of cleanliness and order, as will the utensils used in them, and for
no reason will food products be placed next to articles of another nature.
All cold rooms must have appropriate instruments for controlling and recording temperature and relative
humidity.
Article 179
All meats in general (including poultry and game), before being stored in cold rooms containing other
animal products, should be kept for a time in the antechambers, which will also be relatively cold.
The pieces of meat will be introduced in perfect conservation conditions and must be placed on serial
hangers, so that they are separated from each other and do not touch the floor or walls of the chamber.
The fish will be introduced in perfect conditions of hygiene, conservation and placement. Containers
containing fish, eggs, fruits and other food products must always be in perfect clean condition.
They will be stowed on suitable braces or floorboards to allow convenient circulation of cold air and
sufficient space must be left in the form of central aisles to facilitate passage and the corresponding
control.
It is strictly prohibited to re-conserve frozen meats in cold storage once thawed, and refrigerated meats,
poultry and game meats and eggs removed from them, which have been exposed for some time to the
normal environment, except as necessary to transport it to other cold storage rooms.
Article 180
In general, the conservation of perishable products of animal and plant origin, through artificial cold, will
be carried out in accordance with the instructions herein.
Article 181
Failure to comply with the operating requirements established by the health authority will determine the
intervention of the merchandise contained in the chambers until their suitability for consumption is
determined, without prejudice to the penalties that may apply for non-compliance.
Excepted from this standard are frozen foods and prepared meals, in airtight, inviolable and
bromatologically suitable containers in accordance with the standards established in this Code."
FOOD AUCTIONS
Article 183
The sale at auction or public auction of products whose nutritional conditions are regulated by this
document is subject to the following conditions:
1. They must be previously inspected by the competent health authority; Otherwise, they will be
interdicted or kidnapped, without prejudice to the corresponding penalties.
2. The request for inspection resulting from the provisions of the previous paragraph must be
accompanied by a detailed inventory of the merchandise for sale, specifying the brands of the products,
their nature and quantities per line, singling out the packaging of the products. different size when
available.
3. At the auction, a copy of the inventory indicated in Section 2 must be displayed to the public, signed by
the person responsible for the sale and endorsed by the health authority, with the declaration that said
merchandise is suitable for consumption according to this document.
4. The premises where food products are auctioned will be maintained in adequate sanitary conditions.
5. In the premises referred to in the previous section, the division or transfer of the merchandise subject
to auction will not be permitted.