P1025_CFS Attach_ A1_Chapters 1_5
P1025_CFS Attach_ A1_Chapters 1_5
Code Revision
Australia New Zealand Food Standards Code
Volume 1, Chapters 1 to 5
Contents
Chapter 1—Introduction and standards that apply to all
foods 1
Part 1—Preliminary 1
Division 1—Status of Code ..................................................................... 1
1.01 Name .....................................................................................................1
1.02 Commencement ....................................................................................1
1.03 Overview ...............................................................................................1
Division 2—Interpretation ....................................................................... 2
1.04 Application of interpretation legislation..................................................2
1.05 References to other instruments ...........................................................2
1.06 Definitions ..............................................................................................2
1.07 Meaning of RDI and ESSADI ..............................................................13
1.08 Meaning of medical institution .............................................................13
1.09 Phytosterols, phytostanols and their esters ........................................15
1.10 Units of measurement .........................................................................15
1.11 Meaning of average quantity ...............................................................16
1.12 Compliance with requirements relating to warning statements ..........16
Division 3—Application of Code and effect of variations to Code .... 16
1.13 Application of Code .............................................................................16
1.14 Effect of variations to Code .................................................................17
Part 2—Basic concepts and basic requirements 19
Division 1—Basic concepts .................................................................. 19
1.15 Basic concepts—food..........................................................................19
1.16 Basic concepts—food product ............................................................20
1.17 Basic concepts—ingredient and compound ingredient .......................20
1.18 Basic concepts—component ...............................................................21
1.19 Basic concepts—used as a nutritive substance ..................................21
1.20 Basic concepts—sell ...........................................................................21
Division 2—Basic requirements ........................................................... 24
1.21 Requirements relating to food product on sale ...................................25
1.22 Requirements relating to food product on importation ........................27
1.23 Operation of compositional requirements ...........................................27
1.24 Other requirements relating to food ....................................................28
1.25 Identity and purity ................................................................................28
Part 3—Labelling and other information requirements 29
1.01 Name
This instrument is the Australia New Zealand Food Standards Code.
Note 1: This Code is a standard under the Food Standards Australia New Zealand
Act 1991 (Cth). See also subsection 1.13(3).
Note 2: The provisions of this Code that apply in New Zealand are incorporated
by reference into a food standard under the Food Act 1981 (NZ). See also
subsection 1.13(2).
1.02 Commencement
This Code commences on …………………
Note: This Code repeals and replaces the earlier version. Transitional provisions
are set out in Chapter 5.
1.03 Overview
This Code is structured as follows:
(a) Chapter 1 contains:
(i) preliminary material; and
(ii) provisions that apply to all foods;
(b) Chapter 2 contains provisions that apply only to particular
classes of foods;
(c) Chapter 3 deals with food hygiene, and applies in Australia
only;
(d) Chapter 4 deals with the primary production of food, and applies
in Australia only;
(e) Chapter 5 revokes standards 1.1.1 to 2.10.3 and deals with
transitional matters;
(f) Schedules are set out after Chapter 5.
Note: Chapters 1 and 2 replace standards 1.1.1 to 2.10.3. The remaining
standards are incorporated by reference in Chapters 3 and 4. It is expected
that future variations of this Code will result in these standards being
revoked and incorporated into this instrument.
Division 2—Interpretation
1.06 Definitions
(1) A term used in the Code that is also used in the FSANZ Act has the
same meaning as in the FSANZ Act, unless the contrary intention
appears.
(2) In this Code, unless the contrary intention appears, the following
definitions apply:
agvet chemical—see section 1.144
altered characteristics—see section 1.154.
amino acid modified food—see section 2.153.
AS/NZS means a joint Australia New Zealand Standard published by
Standards Australia.
application Act means an or Ordinance of a jurisdiction under which
the requirements of this Code are applied in the jurisdiction.
AS means an Australian Standard published by Standards Australia.
import includes:
(a) in Australia—import from New Zealand; and
(b) in New Zealand—import from Australia.
individual portion pack—see subsection 1.31(4).
infant formula product—see section 2.82.
infant formula—see section 2.82.
infant means a person under the age of 12 months.
ingredient—see section 1.17.
instant coffee means the dried soluble solids prepared from the water
extraction of coffee.
instant tea means dried soluble solids prepared from the water
extraction of tea.
intra company transfer—see section 1.43.
inulin-derived substance means a mixture of polymers of fructose
with predominantly β (2→1) fructosyl-fructose linkages, with or
without a terminal glucose molecule and includes inulin, but does not
include those polymers of fructose produced from sucrose by
enzymatic action.
iodised salt means a food that may be sold as iodised salt under
section 2.162.
irradiation—see section 1.160.
jam means a food that may be sold as jam under section 2.23.
juice blend—see section 2.42.
jurisdiction means a State or Territory of Australia, or New Zealand.
kava—see section 2.55.
label—see section 1.27.
labelling—see section 1.27.
liqueur means a food that may be sold as liqueur under section 2.73.
lot means a quantity of a food that the manufacturer or producer
identifies as having been prepared, or from which foods have been
packaged or otherwise separated for sale, under essentially the same
conditions, for example:
(a) from a particular preparation or packing unit; and
(b) during a particular time ordinarily not exceeding 24 hours.
tea means the dried or fermented leaves and leaf buds of one or more
of varieties and cultivars of Camelia sinensis (L.) O. Kuntz.
total plant sterol equivalents content—see section 1.09.
trans fatty acids—see section 1.71.
transportation outer means a container or wrapper which:
(a) encases packaged or unpackaged food products for the purpose
of transportation and distribution; and
(b) is removed before the food product is used or offered for retail
sale or which is not taken away by the purchaser of the food
product.
unit quantity means:
(a) for a food product consisting of a solid or semi-solid food—100
grams; or
(b) for a food product consisting of a beverage or other liquid
food—100 millilitres.
use-by date—see section 1.65.
used as a food additive—see section 1.122.
used as nutritive substance—see section 1.19.
used as a processing aid:
(a) in relation to a food—see subsection 1.131(2), and
(b) in relation to a substance—see subsection 1.131(1).
vegetable juice means a food that may be sold as vegetable juice
under section 2.42.
vegetable wine means a food that may be sold as vegetable wine under
section 2.70.
vinegar means a food that may be sold as vinegar under section 2.158.
warning statement, for a food product, means a statement about a
particular aspect of the food that is required to be expressed in the
words set out in the following provisions:
(a) section 1.56 (warning statement relating to royal jelly);
(b) section 2.57 (warning statement relating to kava);
(c) subsection 2.98(1) or section 2.92 (warning statements for infant
formula product);
(d) paragraph 2.110(3)(c) or 2.111(1)(b) (warning statements for
food for infants);
(e) subparagraph 2.129(1)(a)(iii) or 2.129(1)(a)(iv) (warning
statements for formulated supplementary sports food).
white sugar means a food that may be sold as white sugar under
section 2.77.
wholegrain:
(a) wholegrain, as the name of a food, has the meaning given in
subsection 2.02(2); and
(b) a food is a wholegrain food if it may be sold as consisting of, or
containing, wholegrain under subsection 2.02(1).
wholemeal:
(a) wholemeal, as the name of a food, has the meaning given in
subsection 2.02(2); and
(b) a food is a wholemeal food if it may be sold as consisting of, or
containing, wholemeal under subsection 2.02(1).
wine product—see section 2.71.
wine means a product that may be sold as wine under section 2.72.
yoghurt means a food that may be sold as yoghurt under section 2.32.
(b) manufacture, prepare for sale, or sell any food in New Zealand, or import any
food into New Zealand, unless the person and the food comply with all
applicable provisions of the Code relating to:
(i) food safety; and
(ii) the composition of food; and
(iii) the manufacture of food or, as the case may be, the preparation of
food for sale; or
(c) sell or import any food that does not comply with all applicable provisions of
the Code relating to the labelling of food; or
(d) advertise or promote any food unless that person complies with all applicable
provisions of the Code relating to the advertising or promotion of food; or
(e) sell, or import into New Zealand, any material, container, appliance, or
utensil used, or designed for use, in relation to food, unless the material,
container, appliance, or utensil complies with all applicable provisions of the
Code; or
(f) otherwise act in contravention of, or fail to comply with, any provisions of
the Code relating to food manufactured or prepared for sale or sold in New
Zealand, or imported into New Zealand.
Compositional requirements
(2) Subject to this section, the food product may consist of, or have as an
ingredient, any food.
(3) The food product must not consist of, or have as an ingredient or a
component, any of the foods or substances listed in column 1 of the
table to this subsection, unless expressly permitted by a provision
listed in column 2, or another provision of this Code.
(4) The food product must not consist of, or have as an ingredient or a
component, a substance that is used for any of the purposes listed in
column 1 of the table to this subsection, unless expressly permitted by
a provision listed in column 2, or another provision of this Code:
Packaging requirements
(7) If a packaging requirement of this Code applies to the sale of the food
product, the packaging must comply with the requirement.
Labelling requirements
(8) If a labelling requirement of this Code applies to the sale of the food
product, the labelling must comply with the requirement.
Information provision requirements
(9) If an information provision requirement of this Code applies to the
sale of the food product, the information must be provided as required.
(3) If the food product has more than 1 layer of packaging and
subsection (2) requires it to bear a label, only 1 label is required in
relation to the food product.
Note: See also section 1.50.
1.34 Information requirements for food product that does not need to
bear a label
(1) This section applies to a food product that is not required to bear a
label because of section 1.31.
Information that must accompany or be displayed in connection with
the sale of the food product
(2) The information specified in subsection (3) must, in accordance with
the provisions indicated, be stated in labelling that:
(a) accompanies the food product; or
(b) is displayed in connection with the sale of the food product.
(3) For subsection (2), the information is:
(a) any warning statement required by section 1.56;
(b) information relating to irradiated food (see section 1.167).
Information that must accompany food product
(4) The following information must be stated in labelling that
accompanies the food product, in accordance with the provisions
indicated:
(a) if the food product is not required to bear a label because of
subsection 1.31(1)—the information related to storage
conditions required by paragraph 1.69(b); and
(b) in any case—the information related to storage conditions
required by paragraph 1.69(c).
Information that must be displayed in connection with the sale of the
food product
(5) If the food product is not required to bear a label because of
subsection 1.31(1), the following information must be stated in
labelling that is displayed in connection with the display of the food
product, in accordance with the provisions indicated:
(a) information relating to foods produced using gene technology
(see section 1.156);
(b) for fermented comminuted processed or manufactured meat—
the prescribed name (see sections 2.12 and 2.13);
(c) for a food product that consists of kava root:
(i) any statements relating to kava (see section 2.57); and
(ii) the name and address of the supplier (see section 1.54);
Information that must be provided to the purchaser
(6) The following information must be provided to the purchaser, in
accordance with the provisions indicated:
(a) any required statement indicating the presence of offal (see
section 2.09);
(b) for raw meat joined or formed into the semblance of a cut of
meat—any required information relating to that meat (see
section 2.11);
(c) for formed or joined fish—any required information relating to
that fish (see section 2.20).
Information that may either accompany or be displayed with the food
product or which must be provided to the purchaser on request
(7) The information specified in subsection (8) must, in accordance with
the provisions indicated, be stated in labelling that is:
(a) displayed in connection with the display of the food product; or
(b) provided to the purchaser on request.
(8) For subsection (7), the information is:
(a) name of food (see section 1.52);
(b) any advisory statements and declarations (see sections 1.55 and
1.57);
(c) information relating to nutrition, health and related claims (see
subsection 1.95(4));
(d) the information required for a nutrition information panel (see
sections 1.100 and 1.109);
(e) if the food product that is not required to bear a label because of
subsection 1.31(1) or 1.31(2)(a)—information about
characterising ingredients and characterising components
(section 1.111);
(f) for minced meat—if required, the maximum proportion of fat in
the minced meat (see section 2.10);
(g) for formulated caffeinated beverages—any advisory statements
(section 2.61).
(2) If this Code includes a definition of a particular food, that fact alone
does not establish that the defined term is the name of the food for this
section.
(b) wheat, rye, barley, oats and spelt and hybridised strains of those
cereals (that is, cereals and cereal products containing gluten),
other than where these substances are present in beer or spirits;
(c) any of the following foods, or products of those foods:
(i) crustacea;
(ii) egg;
(iii) fish, except for isinglass derived from swim bladders and
used as a clarifying agent in beer or wine;
(iv) milk;
(v) peanuts;
(vi) soybeans;
(vii) sesame seeds;
(viii) tree nuts, other than coconut from the fruit of the palm
Cocos nucifera.
(2) For subsection (1), the food may be present as:
(a) an ingredient or an ingredient of a compound ingredient; or
(b) a substance used as a food additive, or a component of such a
substance; or
(c) a substance or food used as a processing aid, or a component of
such a substance or food.
Note: The labelling provisions are set out in Division 1.
where:
X is the weight of the water, or of the volatile ingredient, that is added
to the food.
Y is the sum of the weight of the water, or of the volatile ingredient,
that is removed and the amount that is used for reconstitution of
dehydrated or concentrated ingredients during preparation,
manufacture or handling of the food.
(5) A compound ingredient may be listed in a statement of ingredients by
listing, in accordance with subsection (1):
(a) the compound ingredient by name as an ingredient of the food,
in accordance with subsection (6); or
(b) each ingredient of the compound ingredient individually as an
ingredient of the food.
(6) If a compound ingredient is listed in accordance with paragraph (5)(a),
it must be followed by a list, in parentheses, of:
1.65 Definitions
In this Division:
baked-for date, in relation to bread, means:
(a) if the time at which the bread was baked is more than 12 hours
before the commencement of the following day—the baked-on
date;
(b) if the time at which the bread was baked is less than 12 hours
before the commencement of the following day—the day after
the baked-on date.
Note: For example, bread that is baked after midday on one day may
have a ‘baked-for date’ of the following day.
baked-on date, in relation to bread, means the date on which the bread
was baked.
best-before date, for a food product, means the date up to which the
food product will remain fully marketable and will retain any specific
qualities for which express or implied claims have been made, if the
food product:
(a) remains in an intact package during its storage; and
(b) is stored in accordance with any storage conditions applicable
under section 1.69.
use-by date, for a food product, means the date after which the
supplier estimates that the food product should not be consumed
because of health or safety reasons, if the food product:
(a) remains in an intact package during its storage; and
(b) is stored in accordance with any storage conditions applicable
under section 1.69.
(5) The day, month and year must be expressed so that they are clearly
distinguishable from each other.
(6) To avoid doubt, subsection (1) does not prevent the addition of a
packed-on date or a manufacturer’s or a packer’s code on the label on
a package of food.
1.70 Outline
This Division:
(a) sets out:
(i) the claims that may be made on labels or in advertisements
about the nutritional content of food (described as
‘nutrition content claims’); and
(ii) the claims that may be made on labels or in advertisements
about the relationship between a food or a property of a
food, and a health effect (described as ‘health claims’);
and
(b) describes the conditions under which such claims may be made;
and
(c) describes the circumstances in which endorsements may be
provided on labels or in advertisements.
general level health claim means a health claim that is not a high
level health claim.
gluten means the main protein in wheat, rye, oats, barley, triticale and
spelt relevant to the medical conditions coeliac disease and dermatitis
herpetiformis.
glycaemic index (GI) means a measure of the blood glucose raising
ability of the digestible carbohydrates in a given food as determined
by a recognised scientific method.
health claim means a claim which states, suggests or implies that a
food or a property of food has, or may have, a health effect.
Note: See also subsection 2.163(3).
(a) of the same type as the food for which the claim is made and
that has not been further processed, formulated, reformulated or
modified to increase or decrease the energy value or the amount
of the nutrient for which the claim is made; or
(b) a dietary substitute for the food in the same food group as the
food for which the claim is made.
saturated fatty acids means the total of fatty acids containing no
double bonds.
serious disease means a disease, disorder or condition which is
generally diagnosed, treated or managed in consultation with or with
supervision by a health care professional.
special purpose food means any of the following:
(a) infant formula product;
(b) food for infants;
(c) a formulated meal replacement;
(d) a formulated supplementary food;
(e) a formulated supplementary sports food;
(f) food for special medical purposes.
sugars means monosaccharides and disaccharides.
Note: In this Division and Division 8, sugars has a narrower meaning than
elsewhere in this Code. See section 1.06 for the general meaning of the
term.
trans fatty acids means the total of unsaturated fatty acids where one
or more of the double bonds are in the trans configuration.
vegetable:
(a) means the edible portion of a plant or constituents of the edible
portion that are present in the typical proportion of the whole
vegetable (with or without the peel or water); and
(b) does not include nuts, spices, herbs, fungi, dried legumes
(including dried legumes that have been cooked or rehydrated)
and seeds.
(v) potassium;
(vi) protein;
(vii) carbohydrate;
(viii) fat;
(ix) the components of any one of protein, carbohydrate or fat;
(x) salt;
(xi) sodium;
(xii) vitamins; or
(b) glycaemic index or glycaemic load;
that does not refer to the presence or absence of alcohol, and is not a
health claim.
Note: See also subsections 2.47(4) and 2.163(3).
(4) Despite paragraph (1)(a), a special purpose food does not need to meet
the NPSC.
(5) In this Subdivision:
general level health claims table means the table to section S4.03 of
Schedule 4.
high-level health claims table means the table to section S4.02 of
Schedule 4.
(6) Despite paragraph (3)(b), if the form of the food to which the claim
relates is the food as sold, the form of the food to which the claim
relates need not be stated.
Subdivision F—Endorsements
(b) the supplier upon request by the relevant authority, makes the
required records available for inspection within the time
specified by the relevant authority; and
(c) the endorsement complies with section 1.77; and
(d) the endorsing body complies with section 1.92.
(2) If a label on, or an advertisement for, imported food makes or includes
an endorsement, the importer of the food must:
(a) keep the required records for the information period as if the
importer of the food were the supplier of the food; and
(b) upon request by the relevant authority, make the required
records available for inspection within the time specified by the
relevant authority.
(3) An endorsement must not refer to a serious disease except in a
reference to the endorsing body if the serious disease is part of the
name of the endorsing body.
(4) This Division, other than sections 1.71, 1.72 and 1.77, do not apply in
relation to an endorsement.
(5) In this section:
information period, in relation to food, means the period:
(a) during which the food is available for sale or advertised for sale;
and
(b) the period of 2 years after the food was last sold, or advertised
or available for sale, whichever is the latest.
required records means a document or documents that demonstrate
that:
(a) a supplier using an endorsement has obtained the permission of
the endorsing body to use the endorsement; and
(b) the endorsing body has a nutrition- or health-related function or
purpose; and
(c) the endorsing body is a not-for-profit entity; and
(d) the endorsing body is not related to the supplier using the
endorsement.
1.97 Purpose
This Division sets out nutrition information requirements in relation to
food products that are required to be labelled under this Code, and for
food products that are exempt from these labelling requirements. This
Division sets out when nutritional information must be provided, and
the manner in which such information must be provided.
Note: Division 7 also sets out additional nutrition information requirements in
relation to nutrition content claims and health claims. This Division does
not apply to infant formula product. Division 1 of Part 9 of Chapter 2 sets
out specific nutrition labelling requirements for infant formula product.
1.110 Definitions
(1) In this Division, in relation to a food product:
characterising component means a component of the food that:
(a) is mentioned in the name of the food; or
(b) is likely to be associated with the name of the food by a
consumer; or
(c) is emphasised on the label of the food product in words, pictures
or graphics.
characterising ingredient means an ingredient or a category of
ingredients of the food that:
(a) is mentioned in the name of the food; or
(b) is likely to be associated with the name of the food by a
consumer; or
(c) is emphasised on the label of the food product in words, pictures
or graphics.
(2) Despite subsection (1), any of the following is not a characterising
ingredient:
(a) an ingredient or category of ingredients that is used in small
quantities to flavour the food; or
(b) an ingredient or category of ingredients that comprises the
whole of the food; or
(c) an ingredient or category of ingredients that is mentioned in the
name of the food but which is not such as to govern the choice
of the consumer, because the variation in the quantity is not
essential to characterise the food, or does not distinguish the
food from similar foods.
(3) Compliance with labelling requirements elsewhere in this Code does
not of itself constitute emphasis for the purposes of this section.
1.121 Outline
This Part sets out the conditions for:
(a) the addition to a food of substances that are not normally
consumed (see Division 2, Division 3 and Division 4); and
(b) the presence in a food of substances that are not normally
consumed (see Division 5, Division 6, Division 7 and Division
10); and
(c) the use of novel foods (see Division 8); and
(d) the use of food produced by gene technology (see Division 9).
1.122 Interpretation
Meaning of used as a food additive
(1) For this Code, a substance is used as a food additive in relation to
food if:
(a) it is a substance identified in subsection (2); and
(b) it is added to the food to perform 1 or more of the technological
purposes listed in Schedule 14.
(2) For subsection (1), the substances are:
(a) any of the following:
(i) a substance that is listed in Schedule 15;
(ii) an additive permitted at GMP;
(iii) a colouring permitted at GMP;
(iv) a colouring permitted to a maximum level; and
(b) any substance that:
(i) has been extracted, refined, or synthesised; and
(ii) is not normally sold as a food product; and
(iii) is not normally used as an ingredient by consumers.
Other definitions
(3) In this Code:
additive permitted at GMP means a substance that is listed in section
S16.01 of Schedule 16.
Note: See subsection 1.124(1).
level in the final food complies with the maximum permitted level in
Schedule 15.
(6) For this Division:
(a) annatto and annatto extracts include norbixin and bixin,
calculated as bixin;
(b) benzoic acid and its salts are calculated as benzoic acid;
(c) cyclamate and its salts are calculated as cyclohexyl-sulphamic
acid;
(d) ethyl lauroyl arginate is calculated as ethyl-Nα-lauroyl-L-
arginate.HCl;
(e) nitrates refers to the total of nitrates and nitrites, calculated as
sodium nitrite;
(f) ferrocyanides are calculated as the total of sodium ferrocyanide
and potassium ferrocyanide;
(g) propionic acid and its salts are calculated as propionic acid;
(h) saccharin and its calcium and sodium salts are calculated as
saccharin;
(i) sorbic acid and its salts are calculated as sorbic acid;
(j) steviol glycosides are calculated as steviol equivalents in
accordance with subsection (7);
(k) sulphur dioxide and sulphites, including bisulphites and
metabisulphites, are calculated as sulphur dioxide.
(7) To calculate the steviol equivalent levels for a steviol glycoside, the
following equation is used:
[SE] CF [SG]
where:
CF is the conversion factor, as follows:
(a) dulcoside A—0.40;
(b) rebaudioside A—0.33;
(c) rebaudioside B—0.40;
(d) rebaudioside C—0.33;
(e) rebaudioside D—0.28;
(f) rebaudioside F—0.34;
(g) rubusoside—0.50;
(h) steviol—1.00;
(i) steviolbioside—0.50;
(j) stevioside—0.40.
[SG] is the concentration of individual steviol glycoside.
[SE] is the concentration as steviol equivalents.
where:
Conci is the concentration of the ith food additive in the food.
MPLi is the maximum permitted level of the ith food additive in the
food.
N is the number of substances used as food additives in the food that
perform the same technological purpose.
where:
Qi, for a particular ingredient, is:
(a) for an unfortified ingredient—the average quantity of the
vitamin or mineral present in the amount of the ingredient in a
reference quantity of the food; and
(b) for a fortified ingredient—the maximum amount that may be
claimed for that vitamin or mineral in the amount of the
ingredient in a reference quantity of the food.
(3) Then, Mrq is rounded to the nearest 2 significant figures.
Subdivision A—Interpretation
(3) For subsections (1) and (2), the substances are the following:
(a) a substance that is listed in Schedule 18;
(b) an additive permitted at GMP.
Note: ‘additive permitted at GMP’ is a defined term—see section 1.122.
1.135 Enzymes
An enzyme listed in section S18.03 of Schedule 18 may be used as a
processing aid to perform any technological purpose if the enzyme is
derived from the corresponding source specified in the table.
Note 1: Section S18.03 includes:
enzymes of animal origin; and
1.144 Interpretation
(1) In this Code:
agvet chemical means an agricultural chemical product or a veterinary
chemical product, within the meaning of the Agvet Code.
Note: The Agvet Code is the Code set out in the Schedule to the Agricultural
and Veterinary Chemicals Code Act 1994 (Cth). See subsection 4(1) of
the FSANZ Act.
(2) Maximum residue limits and extraneous residue limits apply to the
portion of foods specified in Schedule 22.
(3) Unless a maximum residue limit or extraneous limit is specified for a
processed food, the same limit applies to both the processed and the
unprocessed food.
(4) For this Division, a reference to a particular food is to the food as
described in Schedule 22.
1.147 Interpretation
In this Code:
coca bush means:
(a) eurythroxylum coca; or
(b) a substance derived from eurythroxylum coca.
prohibited plant or fungus means:
(a) a plant or fungus listed in Schedule 23; or
(b) a part or a derivative of such a plant or fungus; or
(c) a substance derived from a plant, fungus, part or derivative
referred to in paragraph (a) or (b).
restricted plant or fungus means:
(a) a plant or fungus listed in Schedule 24; or
(b) a part or a derivative of such a plant or fungus; or
(c) a substance derived from a plant, fungus, part or derivative
referred to in paragraph (a) or (b).
1.151 Definitions
In this Code:
non-traditional food means:
(a) a food that does not have a history of human consumption in
Australia or New Zealand; or
(b) a substance derived from a food, where that substance does not
have a history of human consumption in Australia or New
Zealand other than as a component of that food; or
(c) any other substance, where that substance, or the source from
which it is derived, does not have a history of human
consumption as a food in Australia or New Zealand.
novel food means a non-traditional food that requires an assessment of
the public health and safety considerations having regard to:
(a) the potential for adverse effects in humans; or
(b) the composition or structure of the food; or
(c) the process by which the food has been prepared; or
(d) the source from which it is derived; or
(e) patterns and levels of consumption of the food; or
(f) any other relevant matters.
Note: Possible categories of novel foods are described in guidelines issued by
FSANZ. Categories of novel foods may include, but are not limited to, the
following:
plants or animals and their components;
plant or animal extracts;
herbs, including extracts;
dietary macro-components;
single chemical entities;
microorganisms, including probiotics;
foods produced from new sources, or by a process not previously
applied to food.
(a) the novel food is listed in the table to section S25.01 of Schedule
25; and
(b) any conditions of use specified in the corresponding row of that
table are complied with.
1.154 Definitions
In this Code:
altered characteristics: a food produced using gene technology is
taken to have altered characteristics if:
(a) the genetic modification has resulted in one or more significant
composition or nutritional parameters having values outside the
normal range of values for existing counterpart food not
produced using gene technology; or
(b) the level of anti-nutritional factors or natural toxicants are
significantly different in comparison to the existing counterpart
food not produced using gene technology; or
(c) the food produced using gene technology contains a new factor
known to cause an allergic response in particular sections of the
population; or
(d) the intended use of the food produced using gene technology is
different to the existing counterpart food not produced using
gene technology.
food produced using gene technology means a food which has been
derived or developed from an organism which has been modified by
gene technology.
Note: This definition does not include food derived from an animal or other
organism which has been fed food produced using gene technology,
unless the animal or other organism is itself a product of gene technology.
(5) To avoid doubt, if this section does not apply to a food product, this
Code does not require any statement about the genetic status of the
food.
(6) In this section:
novel DNA means DNA which has been modified by the use of gene
technology.
novel protein means protein encoded from novel DNA and, in the
case of a substances used as a processing aid, which has a different
amino acid sequence from that found in nature.
1.157 Interpretation
(1) In this Division:
SPC means a standard plate count at 30C with an incubation time of
72 hours.
(2) In this Division, references to the SPC for powdered infant formula
with added lactic acid producing microorganisms are to the SPC prior
to the addition of the microorganisms to the food.
Subdivision A—Preliminary
1.160 Definitions
In this Code:
irradiation, in relation to food, means subjecting the food to ionising
radiation, other than ionising radiation imparted to food by measuring
or inspection instruments, and irradiate and irradiated have
corresponding meanings.
1.166 Record-keeping
(1) A person who irradiates food must keep records in relation to:
(a) the nature and quantity of the food treated; and
(b) the lot identification; and
(c) the minimum durable life of the food treated; and
(d) the process used; and
(e) compliance with the process used; and
(f) the minimum and maximum dose absorbed by the food; and
(g) an indication whether or not the product has been irradiated
previously and if so, details of such treatment; and
(h) the date of irradiation.
(2) The records must be kept at the facility where the food was irradiated.
(3) The records must be kept for a period of time that exceeds the
minimum durable life of the irradiated food by 1 year.
2.06 Definitions
In this Code:
cured and/or dried meat flesh in whole cuts or pieces means meat
flesh including any attached bone containing no less than 160 g/kg
meat protein on a fat free basis.
manufactured meat means processed meat containing no less than
660 g/kg of meat.
meat:
(a) means the whole or part of the carcass of any of the following
animals, if slaughtered other than in a wild state:
(i) buffalo, camel, cattle, deer, goat, hare, pig, poultry, rabbit
or sheep;
(ii) any other animal permitted for human consumption under
a law of a State, Territory or New Zealand; and
(b) does not include:
(i) fish; or
(ii) avian eggs; or
(iii) foetuses or part of foetuses.
meat flesh means meat that consists of skeletal muscle and any
attached:
(a) animal rind; or
(b) fat; or
(c) connective tissue; or
(d) nerve; or
(e) blood; or
(f) blood vessels; or
(g) skin, in the case of poultry.
offal:
(a) includes blood, brain, heart, kidney, liver, pancreas, spleen,
thymus, tongue and tripe; and
(b) excludes meat flesh, bone and bone marrow.
processed meat means a food containing no less than 300 g/kg meat,
which has, either singly or in combination with other ingredients or
2.11 Information about raw meat joined or formed into the semblance
of a cut of meat
For the labelling provisions, for a food that consists of raw meat that
has been formed or joined in the semblance of a cut of meat, whether
coated or not, using a binding system without the application of heat,
the following information is required:
(a) a declaration that the food consists of meat that is formed or
joined; and
(b) in conjunction with that information, cooking instructions that
would result in microbiological safety of the food being
achieved.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
Note: Section 2.15 applies in Australia only. Bovine products imported for sale
in New Zealand are regulated by the New Zealand Food (Prescribed
Foods) Standard 2007 (NZ) and associated import requirements.
Division 2—Eggs
Note: This Division applies in Australia only.
2.18 Traceability
Eggs intended for retail sale or catering sale must be individually
marked with the producers’ or processors’ unique identification.
Division 2—Jam
edible oil spread means a spreadable food composed of edible oils and
water in the form of an emulsion of the type water-in-oil.
Note: Under section 1.06, edible oil spread is defined for the rest of this Code
as a food that may be sold as edible oil spread under this section.
Division 1—Milk
Note: In Australia, milk must be processed in accordance with Standard 4.2.4.
Division 2—Cream
Division 4—Cheese
(c) the tall oil phytosterol ester is added at no less than 70 g/kg and
no more than 90 g/kg.
Division 5—Butter
Note: Under section 1.06, evaporated milk is defined for the rest of this Code as
a food that may be sold as evaporated milk under this section.
2.44 Definitions
In this Code:
formulated beverage means a non-carbonated, ready-to-drink, water-
based flavoured beverage that contains added vitamins or minerals or
both vitamins and minerals, prepared from one or more of the
following:
(a) water;
(b) fruit juice;
(c) fruit purée;
(d) concentrated fruit juice;
(e) concentrated fruit purée;
(f) comminuted fruit;
(g) orange peel extract;
(h) mineral water;
(i) sugars.
mineral water or spring water means ground water obtained from
subterranean water-bearing strata that, in its natural state, contains
soluble matter.
non-alcoholic beverage means:
(a) packaged water; or
(b) a water-based beverage which may or may not contain other
foods, except for alcoholic beverages; or
(c) electrolyte drinks.
(2) For the labelling provisions, a typical analysis that lists the total
concentration of any naturally occurring compound expressed in either
mg/L or parts per million may be included.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
(3) The typical analysis may also include added fluoride provided that
only the total amount of the naturally occurring and added fluoride is
specified.
(4) A typical analysis that complies with subsections (2) and (3) is not a
nutrition content claim for the purposes of section 1.72.
(2) For an electrolyte drink base, the declaration must be based on the
electrolyte drink as ready to drink.
Division 3—Kava
Note 1: Subsection 1.21(3) provides that a food product must not consist of, or have as an
ingredient or a component, kava or any substance derived from kava, unless expressly
permitted by this Division. This Division defines kava and contains the relevant
permissions.
Note 2: In Australia, this Division should be considered in conjunction with the Customs
(Prohibited Imports) Regulations 1956 (Cth) and certain State and Territory restrictions on
the supply of kava which seek to minimise the detrimental effects associated with kava
abuse. Where kava is permitted for supply, the requirements in this Division complement
those restrictions.
2.58 Interpretation
(1) In this Code:
formulated caffeinated beverage means a flavoured non-alcoholic
beverage which contains caffeine and may contain carbohydrates,
amino acids, vitamins and other substances, including other foods, for
the purpose of enhancing mental performance.
(2) In this Division, a reference to caffeine is a reference to the total
quantity of caffeine, whatever its source.
(4) For the labelling provisions, if the beverage has a one-day quantity, an
advisory statement is required that is to the following effect:
‘Consume no more than [amount of one day quantity (as cans, bottles
or mL)] per day’.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
Division 2—Beer
2.70 Compositional requirement for cider, mead, perry, fruit wine and
vegetable wine
(1) A food that is sold on the basis of a representation that it is a fruit
wine, a vegetable wine or ‘mead’ must consist of:
(a) fruit wine, vegetable wine or mead, as appropriate; or
(b) fruit wine, vegetable wine or mead, as appropriate, with the
addition of any of the following:
(i) fruit juice and fruit juice products;
(ii) vegetable juice and vegetable juice products;
(iii) sugars;
(iv) honey;
(v) spices;
(vi) alcohol;
(vii) water.
(2) A food that is sold on the basis of a representation that it is ‘cider’ or
‘perry’ must consist of cider or perry, as appropriate.
(3) In this section:
cider means the fruit wine prepared from the juice or must of apples
and no more than 25% of the juice or must of pears.
fruit wine or vegetable wine:
(a) means a food prepared from the complete or partial fermentation
of fruit, vegetable, grains, cereals or any combination or
preparation of those foods; and
(b) does not include wine or wine product.
mead means the product prepared from the complete or partial
fermentation of honey.
perry means the fruit wine prepared from the juice or must of pears
and no more than 25% of the juice or must of apples.
Note: Under section 1.06, cider, fruit wine, mead, perry and vegetable wine are
defined for the rest of this Code as a food that may be sold as cider, fruit
wine, mead, perry or vegetable wine under this section.
Division 5—Spirit
Division 2—Honey
2.82 Definitions
In this Code:
follow-on formula means an infant formula product that:
(a) is represented as either a breast-milk substitute or replacement
for infant formula; and
(b) is suitable to constitute the principal liquid source of
nourishment in a progressively diversified diet for infants aged
from 6 months.
infant formula means an infant formula product that:
(a) is represented as a breast milk substitute for infants; and
(b) satisfies by itself the nutritional requirements of infants aged up
to 4 to 6 months.
infant formula product means a product based on milk or other edible
food constituents of animal or plant origin which is nutritionally
adequate to serve by itself as the sole or principal liquid source of
nourishment for infants.
medium chain triglycerides means triacylglycerols that contain
predominantly the saturated fatty acids designated by 8:0 and 10:0.
pre-term formula means an infant formula product specifically
formulated to satisfy particular needs of infants born prematurely or of
low birthweight.
protein substitute means:
2.83 Interpretation
Interpretation of compositional requirements
(1) Compositional requirements in this Division apply to:
(a) a powdered or concentrated form of infant formula product that
has been reconstituted with water according to directions; or
(b) an infant formula product in ‘ready to drink’ form.
Calculation of energy, protein and potential renal solute load
(2) For this Division:
(a) energy must be calculated in accordance with section S30.01 of
Schedule 30; and
(b) protein content must be calculated in accordance with the
formula set out in section S30.02 of Schedule 30; and
(c) potential renal solute load must be calculated in accordance with
section S30.03 of Schedule 30.
(6) For the labelling provisions, if a label contains a claim that the infant
formula product is lactose free, low lactose or words of similar import:
(a) the name of food must include the following:
(i) for a formula represented as lactose free—the words
‘lactose free’; and
(ii) for a formula represented as low lactose—the words ‘low
lactose’; and
(b) the following statements are required:
(i) the amount of lactose expressed in g/100 mL; and
(ii) the amount of galactose expressed in g/100 mL.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
(2) Paragraph (1)(d) does not apply to infant formula products for
metabolic, immunological, renal, hepatic or malabsorptive conditions.
(3) For the labelling provisions, directions (in words or pictures) for the
preparation and use of the infant formula product are required, which
instruct that:
(a) each bottle should be prepared individually; and
(b) if a bottle of made up formula is to be stored prior to use, it must
be refrigerated and used within 24 hours; and
(c) potable, previously boiled water should be used; and
(d) if a package contains a measuring scoop—only the enclosed
scoop should be used; and
(e) formula left in the bottle after a feed must be discarded.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
(4) For the labelling provisions, the required statements are ones
indicating that:
(a) for infant formula—the infant formula product may be used
from birth; and
(b) for follow-on formula—the infant formula product should not be
used for infants aged under 6 months; and
(c) subject to subsection (5), it is recommended that infants over the
age of 6 months should be offered foods in addition to the infant
formula product.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
Subdivision F—Guidelines
2.105 Definitions
In this Code:
cereal-based food means food for infants that is based on cereal.
food for infants:
(a) means a food that is intended or represented for use as a source
of nourishment for infants; and
(b) does not include:
(i) infant formula products; or
(ii) formulated meal replacements; or
(iii) formulated supplementary foods; or
(iv) unprocessed fruit and vegetables.
fruit-based food means food for infants that is based on fruit.
2.110 Labelling
(1) This section does not apply to packaged water.
(2) The label on a package of food for infants must not include a
recommendation, whether express or implied, that the food is suitable
for infants less than 4 months old.
(3) For the labelling provisions, the required information relating to
composition is:
(a) a statement indicating the consistency of the food; and
(b) a statement indicating the minimum age, expressed in numbers,
of the infants for whom the food is recommended; and
(c) if the food is recommended for infants between the ages of 4-6
months, in association with the statement required by
paragraph (b), the words ‘Not recommended for infants under
the age of 4 months’; and
(d) if the monosaccharide and disaccharide content of added sugars
and honey is more than 4 g/100 g—the word ‘sweetened’; and
(e) if honey has been used as an ingredient—in association with the
word ‘honey’, the word ‘sterilised’.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
(2) A claim must not be made, whether express or implied, that a food for
infants is a source of protein unless at least 12% of the average energy
content of the food is derived from protein.
2.112 Representations
(1) A food must not be represented as being the sole or principal source of
nutrition for infants.
(2) The label on a package of food for infants must not include a
recommendation that the food can be added to bottle feeds of an infant
formula product.
(2) Food for infants need not comply with the requirement in Division 7
of Part 3 of Chapter 1 to indicate the potassium content of a food in
the nutrition information panel.
(3) The nutrition information panel for food for infants must be set out in
the format set out in section S12.05 of Schedule 12.
(3) The particulars set out in each column of the nutrition information
panel must be expressed as a proportion of the food as reconstituted
according to those directions.
(4) If more than one fluid for preparing the food is nominated in the label:
(a) the particulars set out in the column should be adjusted
according to the first liquid nominated; and
(b) the name of this liquid must be included in the nutrition
information panel.
2.117 Interpretation
In this Division:
serving means a quantity of the food which constitutes one normal
serving when prepared according to manufacturer’s directions or when
the food requires no further preparation before consumption, and in
the case of a formulated meal replacement is equivalent to one meal.
2.127 Definitions
In this Code:
formulated supplementary sports food means a product that is
specifically formulated to assist sports people in achieving specific
nutritional or performance goals.
one-day quantity in relation to formulated supplementary sports food,
means the amount of that food which is to be consumed in one day in
accordance with directions specified in the label.
(c) if more than 30% of the average energy content of the food is
derived from fat—a statement to the effect that the product is a
high fat food and should be used for special fat loading
strategies rather than everyday use.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
2.137 Definitions
(1) In this Division:
inner package, in relation to a food for special medical purposes,
means an individual package of the food that:
(a) is contained and sold within another package that is labelled in
accordance with section 2.144; and
(b) is not designed for individual sale, other than a sale by a
responsible institution to a patient or resident of the responsible
institution.
Example: An example of an inner package is an individual sachet (or sachets) of
a powdered food contained within a box that is fully labelled, being a
box available for retail sale.
Subdivision C—Composition
Subdivision D—Labelling
(g) directions for the use or the storage of the food, if the food is of
such a nature to require such directions for health or safety
reasons;
(h) nutrition information (see section 2.148);
(i) if appropriate, the information required by subsection 2.149(4)
or 2.150(5).
(2) The label must comply with Subdivision F of Division 1 of Part 3 of
Chapter 1.
(2) A claim to the effect that a food for special medical purposes is low
lactose may be made if the food contains not more than 0.3 g of
lactose per 100 g of the food.
(3) A claim to the effect that a food for special medical purposes is
lactose reduced must be accompanied by a declaration of the
proportion by which the lactose content of the food has been reduced.
(4) If a claim in relation to the lactose content of a food for special
medical purposes is made, the information required is the average
quantity of the lactose and galactose in the food, expressed per given
quantity of the food.
Note: See paragraph 2.144(1)(i).
2.153 Meaning of amino acid modified food and special purpose food
(1) In this Division:
amino acid modified food means a special purpose food if, in the
preparation of the food:
(a) there is a restriction in the use of ingredients containing one or
more particular amino acids; or
(b) there is a reduction of the content of one or more particular
amino acids in any of the ingredients of the food.
special purpose food means a food specially processed or formulated
to satisfy particular dietary requirements that exist because of:
(a) a particular physical or physiological condition; or
(b) a specific disease or disorder; or
(c) both such a condition and a disease or disorder;
and are presented as such.
(2) Other than in Subdivision B of Division 3 of Part 9 of Chapter 2
(Formulated meal replacements), a reference in this Code to a special
purpose food is taken to be a reference to formulated meal
replacement.
Note The effect of subsection (2) is that additives permitted in formulated meal
replacements are permitted in special purpose foods. Subsection (2)
exempts special purpose foods from the requirements for minimum levels
for protein, kJ; and the minimum and maximum levels for vitamins and
minerals. The definition of formulated meal replacements is not intended
to be taken literally in relation to special purpose foods. i.e. special
purpose foods are not necessarily intended as a meal replacement.
2.154 Application
(1) This Division applies in relation to food produced in, or imported into,
New Zealand.
(2) Despite subsection (1), this Division does not apply to food produced
in, or imported into, Australia.
(3) This Division ceases to have effect 2 years after the commencement of
any alternative applicable provisions elsewhere in this Code.
2.155 Composition
A special purpose food may contain any of the vitamins and minerals
specified in column 1 of the table to section S30.11 or S30.12 of
Schedule 30.
2.163 Labelling requirement for reduced sodium salt mixtures and salt
substitutes
(1) For the labelling provisions, the required information is a declaration
of the sodium and potassium content, expressed per 100 g.
(2) The label may include a declaration of the percentage reduction of
sodium in the food, relative to salt.
(3) Such a declaration is not a nutrition content claim or a health claim.
Note: The labelling provisions are set out in Division 1 of Part 3 of Chapter 1.
(CaO WO ) (CaC WC )
Ca R
WO
where:
CaO is the original calcium concentration in the chewing gum in mg/g
of chewing gum.
WO is the weight of the original chewing gum in g.
CaC is the residual calcium in the gum after it has been chewed for 20
minutes in mg/g of chewing gum.
WC is the weight of the chewed gum in g.
(2) A claim about the presence of releasable calcium in chewing gum may
be made only if:
(a) the chewing gum contains no more than 0.2% residual sugars;
and
(b) the chewing gum contains no less than 80 mg (10% of the RDI)
of releasable calcium per serve; and
(c) the maximum quantity claimed is no more than 200 mg (25% of
the RDI) of releasable calcium per serve; and
Column 1 Column 2
If food is sold on the basis that it is the food must consist of
‘coffee’ coffee
‘decaffeinated coffee’ decaffeinated coffee
‘decaffeinated instant coffee’ or instant coffee that contains no more
‘decaffeinated soluble coffee’ than 3 g/kg of anhydrous caffeine on a
dry basis.
‘decaffeinated instant tea’ instant tea that contains no more than
‘decaffeinated soluble tea’ 3 g/kg of anhydrous caffeine on a dry
basis.
‘decaffeinated tea’ decaffeinated tea
‘instant coffee’ or ‘soluble coffee’ instant coffee
‘instant tea’ or ‘soluble tea’ instant tea
‘tea’ tea
Note: The terms coffee, decaffeinated coffee, decaffeinated tea, instant coffee,
instant tea and tea are defined in section 1.06.
Column 1 Column 2
‘chocolate’ chocolate
‘cocoa’ cocoa
‘gelatine’ gelatine
Note: The terms cocoa, chocolate and gelatine are defined in section 1.06.
Section 0
Section 5.02 Transitional provisions for repeal of Standard 1.1A.2—Transitional Standard for
Health Claims