SENSODYNE PRONAMEL EXTRA FRESHNESS (MFC03673)

GlaxoSmithKline UK

Revision date : 2021-08-10

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GHS07
Health risk rating 4
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

EC/CAS

231-667-8/7681-49-4

Name of the chemical

Sodium fluoride

Concentration

N/A

General Information

Revision date

2021-08-10

Product name

SENSODYNE PRONAMEL EXTRA FRESHNESS (MFC03673)

Product Synonyms

SENSODYNE PRONAMEL EXTRA FRESH * SENSODYNE PRONAMEL, OPTAMINT 134601

Emergency telephone

VERISK 3E GLOBAL INCIDENT RESPONSE

Icons in SDS

GHS07

Company Information

company name

GlaxoSmithKline UK

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

msds@gsk.com

GHS Information

Signal word

Warning

Hazard Codes

Hazard statements (CLP)

H317

Hazard statements

Code

Statements

H317

May cause an allergic skin reaction

Section 2

2.1 Classification of the substance or mixture

The mixture has been assessed and/or tested for its physical, health and environmental hazards and the following classification applies.

EU Classification

Regulation (EC) No 1272/2008 as amended

Health hazards

Skin sensitisation Category 1 H317 - May cause an allergic skin reaction. Hazard summary May cause an allergic skin reaction. See section 11 of the SDS for additional information on health hazards.

2.2 Label elements

Label according to Regulation (EC) No. 1272/2008 as amended

Contains

OPTAMINT BRIDGE N&A MINT FLAVOR 134601, POTASSIUM NITRATE, Sodium fluoride

Signal word

Warning

Hazard statements

H317 May cause an allergic skin reaction.

Prevention

P261 Avoid breathing mist/vapours. P272 Contaminated work clothing should not be allowed out of the workplace. P280 Wear protective gloves.

Response

P321 Specific treatment (see on this label). P333 + P313 If skin irritation or rash occurs: Get medical advice/attention. P362 + P364 Take off contaminated clothing and wash it before reuse.

Storage

Not available.

Disposal

P501 Dispose of contents/container in accordance with local/regional/national/international regulations.

Supplemental label elements

45.2 % of the mixture consists of component(s) of unknown acute oral toxicity. 49.4 % of the mixture consists of component(s) of unknown acute dermal toxicity. 56.2 % of the mixture consists of component(s) of unknown acute hazards to the aquatic environment. 56.2 % of the mixture consists of component(s) of unknown long-term hazards to the aquatic environment.

2.3 Other hazards

May cause an allergic skin reaction. This mixture does not contain substances assessed to be

vPvB Substances

PBT according to Regulation (EC) No 1907/2006, Annex XIII. The product does not contain components considered to have endocrine disrupting properties according to REACH Article 57(f) or regulation (EU) 2017/2100 or Commission Regulation (EU) 2018/605 at levels of 0.1% or higher. See section 11 of the SDS for additional information on health hazards.

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