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Convenient Storage and Administration With NUVAXOVID.1


On this page, you will learn:

  • How NUVAXOVID is ready to use, with no dilution, mixing, or thawing required1
  • That NUVAXOVID can be stored in a standard refrigerator1
  • Who is eligible for the vaccine

NUVAXOVID arrives ready to use in pre-filled syringes, with no freezing or thawing needed1

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Ready to use—no dilution, mixing, or thawing required

Ships in a carton of 10 pre-filled syringes, each containing 1 dose of 0.5 mL1

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Store in a standard refrigerator

Store pre-filled syringes between 2 to 8 °C (36 to 46 °F)1

Snowflake icon with a cross mark, indicating do not freeze

Can be coadministered with a seasonal flu vaccine

According to the CDC, COVID-19 and flu vaccines can be administered at the same appointment2

Follow the recommended dosing schedule when administering NUVAXOVID1,3,4

For patients aged 65+

Vaccinated with primary series of NUVAXOVID or with any other COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose at least 2 months after receipt of the previous COVID-19 vaccine dose1
  • ACIP recommends patients should receive an additional dose 6 months after the previous dose (minimum interval of 2 months)3

Not previously vaccinated with any COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose1
  • ACIP recommends patients should receive an additional dose 6 months after the previous dose (minimum interval of 2 months)3

For patients aged 12-64 with ≥1 underlying condition

Vaccinated with primary series of NUVAXOVID or with any other COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose at least 2 months after receipt of the previous COVID-19 vaccine dose1

Not previously vaccinated with any COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose1

Are your high-risk patients eligible for NUVAXOVID?

The NUVAXOVID pivotal trial included patients who were high risk for COVID-19 due to underlying conditions, including chronic lung disease, cardiovascular disease, chronic liver disease, severe obesity, and diabetes.1

You can access the FDA's policy position on COVID-19 vaccination to see the list of medical conditions that increase risk of severe COVID-19. For further information, consult your national and local health authorities.

NUVAXOVID uses the same protein-based technology as certain modern flu vaccines.1,5

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You can easily order NUVAXOVID for your practice today!

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Find COVID-19 resources for you and your patients.
 

ACIP = Advisory Committee on Immunization Practices; CDC = Centers for Disease Control and Prevention.

INDICATION

NUVAXOVID is a vaccine indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). NUVAXOVID is approved for use in individuals who are:

  • 65 years of age and older, or
  • 12 years through 64 years of age with at least one underlying condition that puts them at high risk for severe outcomes from COVID-19.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATION
Do not administer NUVAXOVID to individuals with a known history of severe allergic reaction (e.g., anaphylaxis) to any component of NUVAXOVID or to individuals who had a severe allergic reaction (e.g., anaphylaxis) following a previous dose of NUVAXOVID

MANAGEMENT OF ACUTE ALLERGIC REACTIONS
Appropriate medical treatment must be immediately available to manage potential anaphylactic reactions following administration of NUVAXOVID

MYOCARDITIS AND PERICARDITIS
Clinical trials data provide evidence for increased risks of myocarditis and pericarditis following administration of NUVAXOVID. There have been post-marketing reports of myocarditis and pericarditis following administration of NUVAXOVID

SYNCOPE
Syncope (fainting) may occur in association with administration of injectable vaccines, including NUVAXOVID. Procedures should be in place to avoid injury from fainting

ALTERED IMMUNOCOMPETENCE
Immunocompromised persons, including individuals receiving immunosuppressive therapy, may have a diminished immune response to NUVAXOVID

NUVAXOVID may not protect all vaccine recipients

COMMON ADVERSE REACTIONS
The most commonly reported (>10%) solicited adverse reactions included: injection site pain/tenderness, fatigue/malaise, muscle pain, headache, nausea/vomiting, fever, and joint pain

INDICATION

IMPORTANT SAFETY INFORMATION

References

1. NUVAXOVID. Prescribing Information. Novavax, Inc; 2025. 2. Centers for Disease Control and Prevention. Getting a flu vaccine and other recommended vaccines at the same time. September 2024. Accessed February 1, 2026. https://www.cdc.gov/flu/vaccines/coadministration.html 3. Roper LE, Godfrey M, Link-Gelles R, et al. Use of additional doses of 2024-2025 COVID-19 vaccine for adults aged ≥65 years and persons aged ≥6 months with moderate or severe immunocompromise: recommendations of the Advisory Committee on Immunization Practices—United States, 2024. MMWR Morb Mortal Wkly Rep. 2024;73(49):1118-1123. 4. Panagiotakopoulos L, Moulia DL, Godfrey M, et al. Use of COVID-19 vaccines for persons aged ≥6 months: recommendations of the Advisory Committee on Immunization Practices—United States, 2024-2025. MMWR Morb Mortal Wkly Rep. 2024 Sep 19;73(37):819-824. doi:10.15585/mmwr.mm7337e2 5. Centers for Disease Control and Prevention. Recombinant influenza (flu) vaccine. September 9, 2024. Accessed May 7, 2026. https://www.cdc.gov/fl u/vaccine-types/fl ublok-vaccine.html

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