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PREVNAR® 13 Principal Display Panel (pneumococcal 13-valent conjugate vaccine - diphtheria CRM197 protein)

PRINCIPAL DISPLAY PANEL - 0.5 mL Prefilled Syringe Label

NDC 0005-1971-01
Rx only

Pneumococcal 13-valent Conjugate
Vaccine
(Diphtheria CRM197 Protein)

Prevnar 13®

One Dose (0.5 mL)
FOR IM USE ONLY

REFRIGERATE
DO NOT FREEZE
SHAKE WELL

Wyeth Pharm. Inc.
US Govt. License No. 3

LOT:

EXP:

PAA053716

Principal Display Panel - 0.5 mL Prefilled Syringe Label

PRINCIPAL DISPLAY PANEL - 0.5 mL 10 Syringe Carton - MADE IN IRELAND

NDC 0005-1971-02

Rx only

Pneumococcal 13-valent Conjugate Vaccine
(Diphtheria CRM197 Protein)

Prevnar 13®

10 One-Dose (0.5 mL)
Disposable Syringes

FOR INTRAMUSCULAR USE ONLY

Pfizer

PRINCIPAL DISPLAY PANEL - 0.5 mL 10 Syringe Carton - MADE IN IRELAND

PRINCIPAL DISPLAY PANEL - 0.5 mL 10 Disposable Syringe Carton

NDC 0005-1971-02
Rx only

Pneumococcal 13-valent Conjugate Vaccine
(Diphtheria CRM197 Protein)

Prevnar 13®

10 One-Dose (0.5 mL)
Disposable Syringes

FOR INTRAMUSCULAR USE ONLY

Pfizer

Principal Display Panel - 0.5 mL 10 Disposable Syringe Carton

PRINCIPAL DISPLAY PANEL - 0.5 mL 1 Syringe Carton

NDC 0005-1971-05

Rx only

Pneumococcal 13-valent Conjugate Vaccine
(Diphtheria CRM197 Protein)

Prevnar 13®

One Dose (0.5 mL)
Disposable Syringe

FOR INTRAMUSCULAR USE ONLY

Pfizer

PRINCIPAL DISPLAY PANEL - 0.5 mL 1 Syringe Carton
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Resources

website
Prevnar 13 Website for Healthcare Professionals
 
website
Vaccine Recommendations of the Advisory Committee on Immunization Practices (ACIP)
 
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Report Adverse Event
Pfizer Safety

To report an adverse event related to Pfizer-BioNTech COVID-19 Vaccine (also known as COMIRNATY®, COVID-19 mRNA, Vaccine BNT162b2 or BNT162) or Pfizer COVID-19 Treatment (also known as PAXLOVID™ (nirmatrelvir tablets; ritonavir tablets)), and you are not part of a clinical trial* for this product, click the link below to submit your information:

Pfizer Safety Reporting Site

*If you are involved in a clinical trial for either product, adverse events should be reported to your coordinating study site.

If you cannot use the above website or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at
(800) 438-1985.
FDA Medwatch
You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatchor by calling
(800)-332-1088.