FDA.reportPublic FDA data

NDC 84781-871-02 - PureVita Vitamin E

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
84781-871
Requested NDC
84781-871-02
Package NDCs from labels
84781-871-02
Manufacturer
Trivia Pharmaceuticals, LLC
Effective date
2025-03-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PureVita Vitamin E - Trivia Pharmaceuticals, LLCTrivia Pharmaceuticals, LLC2025-03-06Dietary Supplement

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84781-871PUREVITA VITAMIN E (VITAMIN E) LIQUID [TRIVIA PHARMACEUTICALS, LLC]1Unmatched20250309_6b6fa27c-cc56-454a-bd30-938029bcd308.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
84781-871-02ML - Milliliter84781-871147361ef-6607-4f70-a4f1-7a21317f080512025-05-14

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.