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ZARONTIN® Oral Solution Principal Display Panel (ethosuximide)

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Label - 2418-19

ALWAYS DISPENSE WITH
ACCOMPANYING MEDICATION GUIDE

NDC 0071-2418-19

Pfizer

Zarontin®
(Ethosuximide)
ORAL SOLUTION

250 mg per 5 mL

1 Pint (474 mL)
Rx only

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Label - 2418-19

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Carton - 2418-19

ALWAYS DISPENSE WITH
ACCOMPANYING MEDICATION GUIDE

NDC 0071-2418-19

Pfizer

Zarontin®
(Ethosuximide)
ORAL SOLUTION

250 mg per 5 mL

1 Pint (474 mL)
Rx only

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Carton - 2418-19

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Label - 2418-35

ALWAYS DISPENSE WITH
ACCOMPANYING MEDICATION GUIDE

Pfizer
NDC 0071-2418-35

Zarontin®
(Ethosuximide)
ORAL SOLUTION

250 mg per 5 mL

1 Pint (474 mL)
Rx only

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Label - 2418-35

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Carton - 2418-35

ALWAYS DISPENSE WITH
ACCOMPANYING MEDICATION GUIDE

Pfizer
NDC 0071-2418-35

Zarontin®
(Ethosuximide)
ORAL SOLUTION

250 mg per 5 mL

1 Pint (474 mL)
Rx only

PRINCIPAL DISPLAY PANEL - 474 mL Bottle Carton - 2418-35
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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.

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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.