Note: Ingredients listed on restricted chemical lists
EC/CAS
1310-73-2
Name of the chemical
sodium hydroxide
Concentration
1.0-10.0
EC/CAS
7647-01-0
Name of the chemical
Hydrochloric acid
Concentration
N/A
EC/CAS
108-95-2
Name of the chemical
Phenol
Concentration
<1
General Information
Revision date
2025-01-21
Product name
Alhemo (concizumab-mtci) injection
Chemical name
Mixture
1.2.2. Uses advised against
Keep out of reach of children
supplier name
Novo Nordisk Inc
Manufacturer Name
Novo Nordisk Inc
Emergency telephone
+1-800-727-6500
Icons in SDS
Company Information
company name
Novo Nordisk Inc
GHS Information
Signal word
Not required
Section 2
SECTION 2: Hazards identification
(29 CFR 1910.1200) Classification of the chemical
Signal word
Not required
Hazard statements
Not required
Precautionary statements
Not required
Other hazards which do not result in classification
May cause skin and respiratory irritation This is a drug product and should be used in accordance with the instructions for use. The product is tested according to applicable regulations for pharmaceutical products. Contains a pharmacologically active substance Consult the package insert
2.1 Classification of the substance or mixture
This material is not classified as hazardous under U.S. OSHA regulations (29 CFR 1910.1200) (Hazcom 2012) and Canadian WHMIS regulations (Hazardous Products Regulations) (WHMIS 2015). This document has been prepared in accordance with standards for workplace safety, which require the inclusion of all known hazards of the product or its ingredients regardless of the potential risk. Your needs may vary depending upon the potential for exposure in your workplace. The precautionary statements, warnings and hazards included herein may not apply in all cases, such as when the product or device is in its final form and being used to treat the approved medical condition(s) while under the care of a licensed medical professional and in accordance with the FDA-approved Prescribing Inform tion. Refer to FDA-approved Prescribing Information for final marketed products with regard to special storage, handling and administration requirements in the clinical setting.