ZINACEF (CEFUROXIME INJECTION)

GlaxoSmithKline UK

Revision date : 2022-02-17

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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

50-99-7

Name of the chemical

Glucose C6H12O6

Concentration

N/A

General Information

Revision date

2022-02-17

Product name

ZINACEF (CEFUROXIME INJECTION)

Product Synonyms

ZINACEF FROZEN PREMIX 750MG/50ML * ZINACEF FROZEN PREMIX 1.5G/50ML * ZINACEF

Emergency telephone

VERISK 3E GLOBAL INCIDENT RESPONSE

Icons in SDS

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. Caution - Pharmaceutical agent. 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

CEFUROXIME SODIUM, DEXTROSE, SODIUM CITRATE DIHYDRATE

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 instruction 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

2.55 % of the mixture consists of component(s) of unknown acute oral toxicity. 4.28 % of the mixture consists of component(s) of unknown acute dermal toxicity.

2.3 Other hazards

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

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