ULTIVA INJECTION

GlaxoSmithKline UK

Revision date : 2018-10-04

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Health risk rating 1
Safety risk rating 1
Environmental risk rating 1

General Information

Revision date

2018-10-04

Product name

ULTIVA INJECTION

Product Synonyms

ULTIVA INJECTION (1 MG, 2 MG AND 5MG) * REMIFENTANIL POWDER FOR INJECTION *

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Company Information

company name

GlaxoSmithKline UK

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

msds@gsk.com

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

Directive 67/548/EEC or 1999/45/EC as amended Exempt from requirements - product regulated as a medicinal product, cosmetic product or medical device. Regulation (EC) No 1272/2008 as amended Exempt from requirements - product regulated as a medicinal product, cosmetic product or medical device.

2.2 Label elements

Label according to Regulation (EC) No. 1272/2008 as amended Exempt from requirements - product regulated as a medicinal product, cosmetic product or medical device.

2.3 Other hazards

Caution - Potent pharmaceutical agent. See section 11 of the SDS for additional information on health hazards.

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