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Labelling
Labelling
(GHS) has been available since 2003. In Europe, the CLP (Classification, Labelling and
Packaging) Regulation implements this system in the workplace and for consumers. The
Regulation is being gradually applied and will eventually replace the pre-existing European
system in 2015.
After explaining the use of labelling, this article aims to present the scope of the GHS, its
impact in Europe and the current European classification and labelling systems of chemicals.
To alert users to the health and environmental hazards of chemicals, European Regulations
call for the use of safety labels on packaging of these products. These labels also inform users
of the precautions to take to safely handle, store and dispose of the chemicals.
Labelling of chemicals is based on their classification, which involves determining the hazard
category to which the chemical belongs and assigning a codified regulatory phrase describing
the type of hazard (hazard statement according to the CLP regulation, risk phrase in the pre-
existing European regulations) (see chapter 'CLP regulation' below).
There are two types of chemicals according to the Regulations: substances and mixtures (or
preparations, according to the pre-existing European regulations):
Substance means a chemical element and its compounds in the natural state or
obtained by any manufacturing process, e.g. acetone, ethanol, formaldehyde, silica,
sodium hydroxide and chlorine.
Mixtures or preparations are composed of two or more substances, e.g. solutions,
detergents, inks and paints.
Note: In the pre-existing European system of classification and labelling of chemicals (see
chapter 'Pre existing European system below), the term 'danger' was used instead of 'hazard'.
While covering workplaces, transport, consumers and emergency services, the GHS
harmonises:
Twenty-nine hazard classes have been defined, and most of them have been divided into
hazard categories. For example, the GHS divides the flammable liquids class into four
categories. For each hazard class and category, the GHS defines the criteria for classification
and the associated labelling elements: hazard pictogram, signal word, hazard statement and
precautionary statements.
The safety data sheet described in the GHS is mainly based on the European model described
in Directive 91/155/EEC (repealed and replaced by the REACH regulation). It has 16
sections.
The building block approach defined by the GHS enables countries or organisations like the
European Union that adopt this system to choose the building blocks they wish to apply.
They can then use these building blocks to develop a regulatory approach. The GHS
describes what can be considered as building blocks, i.e. hazard classes and hazard
categories, and establishes rules for 'customising' a classification and labelling system so as to
maintain consistency in the application of the GHS.
For several decades in Europe, the classification, labelling and packaging system of
chemicals has been based on two Directives:
Directive 67/548/EEC of 27th June 1967 concerning the classification, packaging and
labelling of dangerous substances as modified[5] (including later amendments)
Directive 1999/45/EC of 31st May 1999 concerning the classification, packaging and
labelling of dangerous preparations as modified (successor to earlier Directives)[6].
These Directives and their subsequent amendments have been transposed into national law
(e.g. two ministerial orders in France) for application in the different Member States of the
European Union.
The pre-existing system is based on the definition of 15 categories of danger, i.e. substances
and preparations that are explosive, oxidising, extremely flammable, highly flammable,
flammable, very toxic, toxic, harmful, corrosive, irritant, sensitising, carcinogenic,
mutagenic, toxic for reproduction and dangerous for the environment.
There is a list of substances (see below) for which the classification and labelling were set at
European level (so-called harmonised classification and labelling) and must be applied in all
Member States. This list is not an exhaustive list of dangerous substances. If no harmonised
classification has been established, the manufacturer, importer or distributor is responsible for
evaluating the dangers and determining the classification of the substance to be placed on the
market. In this case, classification is based on criteria established in regulations and generally
on experimental test results: flash point for determining the flammability of liquids,
LD<sub50 (‘median’ lethal dose in experimental animals) for determining acute toxicity, etc.
According to the pre-existing regulatory system, the labels applied on chemicals must include
in particular the following:
the danger symbols and indications of danger (see Figure 1)[7] that indicate the most
significant dangers posed by the chemical;
the risk phrases:
Examples: R10: flammable; R36: irritating to eyes; R62: risk of impaired fertility;
Examples: S45: In case of accident or if you feel unwell, seek medical advice immediately
(show the label where possible); S53: Avoid exposure – obtain special instructions before
use.
CLP Regulation
Member States requested the European Commission to prepare a proposal for a Regulation
which would adopt the GHS criteria of the United Nations in all EU Member States. In the
workplace and for consumers, the GHS recommendations will be progressively put into
application by EC Regulation 1272/2008 of 16th December 2008[8], referred to as the CLP
(Classification, Labelling and Packaging) Regulation. Many of the international
recommendations were taken into consideration. The first adaptations to technical and
scientific progress were made in 2009, 2011, 2012, June 2013 and August 2012.[8]
The purpose of this Regulation is to harmonise the criteria for classification of substances and
mixtures, and the rules on labelling and packaging for hazardous substances and mixtures. It
also aims at establishing a classification and labelling inventory of substances. This Directive
shall not apply to non-isolated intermediates, waste, medicines, cosmetics, food and feeding
stuffs, and substances and mixtures that are either radioactive, or subjects to custom
supervision, or used for scientific research and are non-marketed. This Regulation shall not
apply to the transport of dangerous goods by air, sea, road, rail or inland waterways except
for labelling of outer packaging, inner packaging and single packaging.[9]
The current European Union CLP Regulation is directly applicable in all Members States and
does not have to be transposed.
Main changes
The most important modifications between the pre-existing European system and the current
CLP Regulation include the following:
The hazard classes are assigned to hazard categories which describe the severity of the effect
(e.g. health hazards are broken down from the highest category 1 to the lowest category 5;
self-reactive substances are assigned to Type A being the most hazardous and Type F being
the least hazardous) (that corresponds to the building blocks).
One the one hand the CLP includes some EU specific Hazard statements compared to the
GHS (e.g. hazardous for the ozone layer), on the other hand the CLP applied the building
block approach so that certain hazard categories that were not in the previous EU
classification legislation have been left out (e.g. flammable liquid, category 4 in GHS is not
part of the CLP).
Changes in the criteria for classification: physical hazard classification is now based
on tests described in international recommendations on the transport of dangerous
goods, mixture classification criteria relative to health hazards are significantly
different, changes have been made to classification thresholds, etc.
Labelling changes: danger symbols and indications of danger have been replaced by
hazard pictograms (Figure 2).
A signal word must generally be shown on the label. The words 'DANGER' (used for the
most severe hazard categories) and 'WARNING' are used.
Risk phrases are replaced by hazard statements associated with an alphanumerical code
consisting of the letter H and 3 digits (see Table 1 below)[8].
Examples:
The wording of the precautionary statements ('safety phrases' in the pre-existing European
system) has been modified as well as the associated codification: the alphanumerical code
consists of the letter P and 3 digits (see Table 2 below)[8].
Examples:
Examples:
CLP inventory
All substances on the EU market on 1 December 2010 should have been notified to the
European Chemicals Agency (ECHA) before the 3 January 2011. New substances should be
notified within one month of their placement on the market to ECHA. This information as
well as the data collected and registered under the REACH Regulation are used to supply a
classification and labelling inventory. As of the end of 2014, ECHA had received 6 million
notifications for more than 120,000 substances.[10] Section V of the CLP Regulation sets out
the provisions for the establishment of and notification to the inventory.
The procedure for harmonisation of classification and labelling of substances described in the
CLP Regulation replaces the pre-existing European procedure.
Table 3: Outline of the CLP Regulation annexes
The list of harmonised classification and labelling for hazardous substances, which was
drawn up for the pre-existing system, is now included in Annex VI of the CLP Regulation [11]
Part 3 of this annex includes two tables:
Table 3.1 includes the list of harmonised classifications and labellings based on the
criteria of the CLP Regulation.
Table 3.2 contains the same information as Table 3.1 but prepared according to the
pre-existing system.
The annex was completed and modified by several adaptations to technical and scientific
progress to the CLP Regulation.[8]. When searching for a classification, these adaptations
must first be consulted, followed by the CLP Regulation.
The following substances shall normally be subject to harmonised classification and labelling
according to the CLP Regulation:
carcinogenic substances;
mutagenic substances;
substances toxic for reproduction;
respiratory sensitisers;
active substances in biocidal or plant protection products;
on a case-by-case basis, substances with other hazard classes than those referred
above if justification can be provided demonstrating the need for such action.
A proposal for harmonised classification and labelling can be submitted to the European
Chemicals Agency (ECHA) by Member State competent authorities, manufacturers,
importers and downstream users.
Application schedule
Until 2017, two types of labels were on the European market; the pre-existing regulatory
system and the system described in the CLP Regulation coexisted during this transition
period. As of 1st December 2010, substance labelling must comply with the CLP Regulation.
But, until 1st June 2015, the two systems of substance classification must have been
mentioned on the safety data sheet.
Concerning mixtures, until 1st June 2015 classification and labelling had to comply with the
pre-existing system, after which the CLP Regulation must have been applied. However, the
CLP Regulation may have been put into application earlier on a voluntary basis. In such
cases, the label should have complied with the CLP Regulation, but the safety data sheet had
to continue to include both the mixture classification under the pre-existing system and the
CLP classification.
Only substances and mixtures placed on the market before 1st December 2010 and 1st June
2015, respectively, could benefit from a re-labelling and re-packaging exemption for 2 years
and could therefore continue to use labelling compliant with the pre-existing system until 1st
December 2012 and 1st June 2017, respectively. However, Directives 67/548/EEC (on
dangerous substances) and 1999/45/EC (on dangerous preparations) were totally repealed in
2015. All labeling must now therefore be compliant with the CLP Regulation.