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Comirnaty LP.8.1 6 months to <5 years (yellow cap) formulation

Details for Comirnaty LP.8.1 6 months to <5 years (yellow cap) vaccine and its components.

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This page was added on 14 November 2024.

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This page was updated on [date-counter-updated-date]. View history of updates

Sponsor
Pfizer Australia
Administration route
Intramuscular injection
Vaccine group
Paediatric formulations
Description:

Registered for use in people aged 6 months - <5 years

COVID-19 vaccine containing nucleoside-modified mRNA encoding the spike glycoproteins of SARS-CoV-2 LP.8.1 strain.

Multi dose vial without preservative containing 0.3 mL of concentrated suspension for injection. Requires dilution with 0.9% sodium chloride. Each vial contains 3 doses (0.3mL per dose after dilution) in 0.48mL.

Each 0.3 mL dose contains:

  • 3 µg mRNA encoding the SARS-CoV-2 LP.8.1 spike glycoprotein
  • ((4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate) (ALC-0315)
  • 2-[(polyethylene glycol)-2000]-N,N-ditetradecylacetamide (ALC-0159)
  • Distearoylphosphatidylcholine (DSPC)
  • Cholesterol
  • Trometamol
  • Trometamol hydrochloride
  • Sucrose
  • Water for injections

For Product Information and Consumer Medicine Information about Comirnaty LP.8.1 visit the Therapeutic Goods Administration website.

Additional vaccine information

For detailed advice on vaccine dosage, administration, contraindications and precautions, and variations from product information, please visit the relevant disease chapter/s.

Related diseases
COVID-19

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https://immunisationhandbook.health.gov.au/vaccines/comirnaty-lp81-6-months-to

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