Home FDA labels 53e9feb6-6a01-a425-e063-6394a90ad978 EUBIOFLOR 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 EUBIOFLOR
Generic name ACTIVATED CHARCOAL - AETHUSA CYNAPIUM - ALTHAEA OFFICINALIS LEAF - BILBERRY - CANDIDA ALBICANS - UNCARIA TOMENTOSA - ESCHERICHIA COLI - INDOLE - MERCURIUS SOLUBILIS - OKOUBAKA AUBREVILLEI BARK - PORK LIVER - PROTEUS VULGARIS - SILYBUM MARIANUM SEED - SKATOLE - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA COLON - SUS SCROFA GALL BLADDER - SUS SCROFA PANCREAS - TABEBUIA IMPETIGINOSA BARK - TARAXACUM OFFICINALE - VERATRUM ALBUM ROOT -
Manufacturer Guna spa
Product type HUMAN OTC DRUG
SPL set ID 7dacc28a-2185-4566-8e83-c7a70338797f
SPL ID 53e9feb6-6a01-a425-e063-6394a90ad978
Version 6
Effective date 2026-06-10
Source export date 2026-10-30
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run 20261102T182004Z
Imported at 2026-11-02 19:30:55 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 · 29 matching rows.
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Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS Stop use and ask doctor if symptoms persist more than 5 days. If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children . In case of overdose, get medical help or contact a Poison Control Center right away. Contains ethyl alcohol 30%
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.