DIMETAPP PSE COUGH COLD & FLU DAY RELIEF

GlaxoSmithKline Australia Phamaceuticals and Vaccines

Revision date : 2020-11-18


GHS07
Health risk rating 4
Safety risk rating 4
Environmental risk rating 5

General Information

Revision date

2020-11-18

Product name

DIMETAPP PSE COUGH COLD & FLU DAY RELIEF

Product Synonyms

ROBITUSSIN COLD & FLU LIQUID CAPS * DEXTROMETHORPHAN HYDROBROMIDE 10 mg, PARACETAMOL 300 mg, PSEUDOEPHEDRINE HYDROCHLORIDE 30 mg Capsule, Liquid Filled

Emergency telephone

VERISK 3E GLOBAL INCIDENT RESPONSE

Icons in SDS

Company Information

Company name

GlaxoSmithKline Australia Phamaceuticals and Vaccines

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

msds@gsk.com

GHS Information

Signal word

Warning

Section 2

Physical hazards

Not classified.

Health hazards

Skin corrosion/irritation Category 2 Serious eye damage/eye irritation Category 2 Sensitization, skin Category 1B

Environmental hazards

Not classified. Label elements, including precautionary statements Hazard symbol(s) Exclamation mark

Signal word

Warning

Hazard statements

Causes skin irritation. May cause an allergic skin reaction. Causes serious eye irritation.

Prevention

Wash thoroughly after handling. Contaminated work clothing should not be allowed out of the workplace. Wear eye protection/face protection. Wear protective gloves.

Response

IF ON SKIN Wash with plenty of soap and water. IF IN EYES Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Specific treatment (see on this label). If skin irritation or rash occurs: Get medical advice/attention. If eye irritation persists: Get medical advice/attention. Take off contaminated clothing and wash before reuse.

Storage

Not available.

Disposal

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

Other hazards which do not result in classification

Occupational Exposure Limits for constituents are listed in Section 8.

Additional information

20.1 % of the mixture consists of component(s) of unknown acute oral toxicity. 86.4 % of the mixture consists of component(s) of unknown acute dermal toxicity. 65.9 % of the mixture consists of component(s) of unknown acute hazards to the aquatic environment. 65.9 % of the mixture consists of component(s) of unknown long-term hazards to the aquatic environment.

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