Gel Etchant

Kerr Italia S.r.l

Revision date : 2022-08-20

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GHS05
Health risk rating 3
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

EC/CAS

231-633-2/7664-38-2

Name of the chemical

phosphoric acid

Concentration

( 10 ≤C < 25) Eye Irrit. 2, H319 ( 10 ≤C < 25) Skin Irrit. 2,...

General Information

Version

6.0

Revision date

2022-08-20

Product name

Gel Etchant

1.2.1 Relevant identified uses

Professional use

Emergency telephone

001-800-424-9300, +1 (703) 527-3887, +353 1 809 2566, +353 1 809 2166, +356 2545 6508, +44 191 2606182, +44 191 2606180

Icons in SDS

GHS05 M004 M009 T031

Company Information

company name

Kerr Italia S.r.l

e-mail address of the competent person responsible for the Safety Data Sheet

safety@envistaco.com

GHS Information

Signal word

Danger

Hazard Codes

Hazard statements (CLP)

H314, H318

Hazard statements

Code

Statements

H314

Causes severe skin burns and eye damage

Section 2

SECTION 2: Hazards identification

According to Regulation (EC) No. 1272/2008 (CLP) Classification of the substance or mixture

Hazard statements

see section 16 : H314 - Causes severe skin burns and eye damage.

Adverse physicochemical, human health and environmental effects

No additional information available

Hazard pictograms

GHS05

Signal word

Danger 1/9

Precautionary statements

P260 - Do not breathe dust/fume/gas/mist/vapours/spray. P264 - Wash hands thoroughly after handling. P280 - Wear eye protection, protective gloves. P301+P330+P331 - IF SWALLOWED: rinse mouth. Do NOT induce vomiting. P303+P361+P353 - IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. P305+P351+P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P310 - Immediately call a POISON CENTER or doctor/physician. P501 - Dispose of contents/container to a hazardous or special waste collection point.

Additional information

The product is seen as a medical device (Directive 90/385/EEC, 93/42/EEC, 98/79/EC) and therefore not subject to labelling (EU-regulation 1272/2008, article 1, paragraph 5d).

Other hazards which do not result in classification

None under normal conditions. This substance/mixture does not meet the PBT criteria of REACH regulation, annex XIII This substance/mixture does not meet the vPvB criteria of REACH regulation, 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 %

2.1 Classification of the substance or mixture

Classification according to Regulation (EC) No. 1272/2008 [CLP] Skin Corr. 1B H314 Eye Dam. 1 H318 Full text of hazard classes and H-statements : see section 16 Adverse physicochemical, human health and environmental effects No additional information available 2.2. Label elements Labelling according to Regulation (EC) No. 1272/2008 [CLP] Hazard pictograms (CLP) : GHS05 Signal word (CLP) : Danger 1/9 Hazard statements (CLP) : H314 - Causes severe skin burns and eye damage. Precautionary statements (CLP) : P260 - Do not breathe dust/fume/gas/mist/vapours/spray. P264 - Wash hands thoroughly after handling. P280 - Wear eye protection, protective gloves. P301+P330+P331 - IF SWALLOWED: rinse mouth. Do NOT induce vomiting. P303+P361+P353 - IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. P305+P351+P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P310 - Immediately call a POISON CENTER or doctor/physician. P501 - Dispose of contents/container to a hazardous or special waste collection point. Extra phrases : The product is seen as a medical device (Directive 90/385/EEC, 93/42/EEC, 98/79/EC) and therefore not

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