General Information
Version
1.0
Revision date
2023-08-21
Product name
Haloperidol decanoate impurity mixture
1.2.2. Uses advised against
Do not use : Ingestion, Inhalation, Dermal
Emergency telephone
+33(0)390215608
Icons in SDS
Company Information
company name
EDQM
e-mail address of the competent person responsible for the Safety Data Sheet
sds@edqm.eu
GHS Information
Signal word
Warning
Hazard Codes
Hazard statements (CLP)
H302, H361d
Hazard statements
Code
Statements
H302
Harmful if swallowed
Section 2
SECTION 2: Hazards identification
Adverse physicochemical, human health and environmental effects
Expert judgement and weight of evidence determination.
2.2 Label elements
Labelling
Hazard pictograms
GHS07 GHS08 GHS08
Signal word
Warning
Contains
Haloperidol undecanoate; Haloperidol octanoate; Haloperidol dodecanoate
Hazard statements
H302 - Harmful if swallowed. H361d - Suspected of damaging the unborn child.
Precautionary statements
P201 - Obtain special instructions before use. P202 - Do not handle until all safety precautions have been read and understood. P264 - Wash hands, forearms and face thoroughly after handling. P270 - Do not eat, drink or smoke when using this product. P280 - Wear protective gloves/protective clothing/eye protection/face protection/hearing protection. P301+P312 - IF SWALLOWED: Call a POISON CENTRE or doctor if you feel unwell. P308+P313 - IF exposed or concerned: Get medical advice/attention. P330 - Rinse mouth. P405 - Store locked up. P501 - Dispose of contents/container to hazardous or special waste collection point, in accordance with local, regional, national and/or international regulation. Labelling according to: exemption for inner packaging where the contents do not exceed 10ml
Hazardous Ingredients
Haloperidol undecanoate; Haloperidol octanoate; Haloperidol dodecanoate
2.3 Other hazards
Contains no PBT/vPvB substances ≥ 0.1% assessed in accordance with REACH Annex XIII The mixture does not contain substance(s) included in the list established in accordance with Article 59(1) of REACH for having endocrine disrupting properties, or is not identified as having endocrine disrupting properties in accordance with the criteria set out in Commission Delegated Regulation (EU) 2017/2100 or Commission Regulation (EU) 2018/605 at a concentration equal to or greater than 0,1 %