Home FDA labels 04a53245-9a12-49fa-e063-6394a90af203 MEB Puri-vega openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name MEB Puri-vega
Generic name MEB PURI-VEGA
Manufacturer Kadesh Incoporation Co,Ltd
Product type HUMAN OTC DRUG
SPL set ID 03865989-3034-10fc-e063-6394a90ac80b
SPL ID 04a53245-9a12-49fa-e063-6394a90af203
Version 2
Effective date 2023-09-05
Source export date 2026-10-12
Source partition 12
Source file https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:56:28 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 18 matching rows.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings Individuals with specific sensitivities to ingredients or allergies should check the list of ingredients before consumption. If your symptoms do not improve and worsen even after 7 days, discontinue use and consult a doctor for further advice.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.