OK PANEL MIX

Empresa AGA S.A. de C.V

Revision date : 2025-01-21

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GHS08
Health risk rating 4
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

EC/CAS

111-46-6

Name of the chemical

diethyleneglycol

Concentration

≥1.0-≤4.8

General Information

Version

4

Revision date

2025-01-21

Product name

OK PANEL MIX

1.2.1 Relevant identified uses

Consumer applications

Manufacturer Name

Empresa AGA S.A. de C.V

Icons in SDS

GHS08 M004 M008 M009 M010 M011 M017

Company Information

company name

Empresa AGA S.A. de C.V

GHS Information

Signal word

Warning

Hazard Codes

Hazard statements (CLP)

H373

Hazard statements

Code

Statements

H373

May cause damage to organs through prolonged or repeated exposure

Section 2

SECTION 2: Hazards identification

Classification of the SPECIFIC TARGET ORGAN TOXICITY (REPEATED EXPOSURE) - Category 2 substance or mixture Percentage of the mixture consisting of ingredient(s) of unknown acute toxicity 51.6% (oral), 51.6% (dermal), 52.9% (inhalation)

Signal word

Warning

Hazard statements

H373 - May cause damage to organs through prolonged or repeated exposure. (kidneys)

Precautionary statements

General P103 - Read label before use. P102 - Keep out of reach of children. P101 - If medical advice is needed, have product container or label at hand.

Prevention

P260 - Do not breathe dust.

Response

P314 - Get medical advice or attention if you feel unwell.

Storage

Not applicable.

Disposal

P501 - Dispose of contents and container in accordance with all local, regional, national and international regulations.

Other hazards which do not result in classification

Sanding and grinding dusts may be harmful if inhaled. Emits toxic fumes when heated. See toxicological information (Section 11)

2.1 Classification of the substance or mixture

SPECIFIC TARGET ORGAN TOXICITY (REPEATED EXPOSURE) - Category 2 substance or mixture Percentage of the mixture consisting of ingredient(s) of unknown acute toxicity: 51.6% (oral), 51.6% (dermal), 52.9% (inhalation)

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