Home FDA labels b2588f62-6cc5-327e-e053-2a95a90aaafb GUNA LYMPHO DETOX 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 LYMPHO DETOX
Generic name AESCULUS HIPPOCASTANUM - APIS MELLIFERA - CALENDULA OFFICINALIS FLOWER - HEXAKETOCYCLOHEXANE - EQUISETUM HYEMALE - FUMARIC ACID - GRAPHITE - HYDRASTIS CANADENSIS - HYDROCOTYLE ASIATICA - JUGLANS REGIA - LEVOTHYROXINE - MAGNESIUM PHOSPHATE - MALIC ACID - MYOSOTIS ARVENSIS - PHYTOLACCA AMERICANA ROOT - SARSAPARILLA - SODIUM DIETHYL OXALACETATE - SODIUM PYRUVATE - SUS SCROFA PLACENTA - TARAXACUM OFFICINALE -
Manufacturer Guna spa
Product type HUMAN OTC DRUG
SPL set ID aeb71e21-2fdb-6b84-e053-2995a90a4c01
SPL ID b2588f62-6cc5-327e-e053-2a95a90aaafb
Version 2
Effective date 2020-10-23
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:47:55 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 · 28 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 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 overdose,seek professional assistance or contact a Poison Control Center immediately. Contains ethyl alcohol 30%
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.