Note: Ingredients listed on restricted chemical lists
EC/CAS
94-36-0
Name of the chemical
Dibenzoyl peroxide
Concentration
N/A
EC/CAS
202-327-6
Name of the chemical
Dibenzoyl peroxide
Concentration
N/A
General Information
Revision date
2017-10-19
Product name
Core.X Flow Catalyst
1.2.1 Relevant identified uses
Core Build-Up Material
1.2.2. Uses advised against
No further relevant information available
Emergency telephone
+49-(0)7531-583-0 8 00 - 17 00 (GMT + 1 00
Icons in SDS
Company Information
company name
Dentsply DeTrey GmbH
e-mail address of the competent person responsible for the Safety Data Sheet
KonstanzDEU.info-sdb@dentsplysirona.com
GHS Information
Signal word
Warning
Hazard Codes
Hazard statements (CLP)
H315, H317, H319
Hazard statements
Code
Statements
H315
Causes skin irritation
Section 2
CLP CLASSIFICATION
Skin Irrit. 2 H315 Causes skin irritation. Eye Irrit. 2 H319 Causes serious eye irritation. Skin Sens. 1 H317 May cause an allergic skin reaction.
2.2 Label elements
Labelling according to Regulation (EC) No 1272/2008 The product is classified and labelled according to the CLP regulation.
Hazard pictograms
GHS07
Hazardous Ingredients
1-methylethylidene)bis[4,1-phenyleneoxy(2-hydroxy-3,1-propanediyl)]bismethacrylate Ethoxylated Bisphenol A Dimethacrylate 2,2'-Ethylendioxydiethyldimethacrylat dibenzoyl peroxide
Hazard statements
H315 Causes skin irritation. H319 Causes serious eye irritation. H317 May cause an allergic skin reaction.
Precautionary statements
P261 Avoid breathing dust/fume/gas/mist/vapours/spray. P280 Wear protective gloves / eye protection / face protection. P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P333+P313 If skin irritation or rash occurs: Get medical advice/attention. P337+P313 If eye irritation persists: Get medical advice/attention. P501 Dispose of contents/container in accordance with local/regional/national/international regulations.
Additional information
As this product is a medical device in the meaning of Directive 93/42/EEC and intended for use by the end consumer and is applied in an invasive manner or body contact, it is exempt from the labelling requirements according to regulation 1272/2008.
PBT Substances
Not applicable
vPvB Substances
Not applicable *
