Home FDA labels ba48694e-5cb1-22ef-e053-2995a90a9965 GUNA HEALTHY BRAIN 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 GUNA HEALTHY BRAIN
Generic name CITRULLUS COLOCYNTHIS FRUIT PULP - UBIDECARENONE - SUS SCRIFA ADRENAL GLAND - SUS SCROFA PLACENTA - SELENIUM - THUJA OCCIDENTALIS LEAFY TWIG - CONIUM MACULATUM FLOWERING TOP - SUS SCROFA EMBRYO - ACONITUM NAPELLUS - ALOE - BARIUM OXALOSUCCINATE - SUS SCROFA CEREBRUM - ARNICA MONTANA - SUS SCROFA HYPOTHALAMUS -
Manufacturer Guna spa
Product type HUMAN OTC DRUG
SPL set ID ba486fa9-53d1-95d9-e053-2995a90af42d
SPL ID ba48694e-5cb1-22ef-e053-2995a90a9965
Version 1
Effective date 2021-02-17
Source export date 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:14 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 · 22 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 WARNINGS Stop use and ask doctor if symptoms worsen or persist more than 5 days. If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children. In case of accidental overdose, seek professional assistance or contact a poison control center immediately. Contains Aloe. Do not use orally for more than 30 days. Contains ethyl alcohol 30%
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.