Home FDA labels af5e38c0-3d5d-4733-e053-2a95a90afefe GUNA DEEP CLEANSE 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 DEEP CLEANSE
Generic name APIS MELLIFERA - BERBERIS VULGARIS ROOT BARK - CHELIDONIUM MAJUS - CHONDRODENDRON TOMENTOSUM ROOT - EQUISETUM HYEMALE WHOLE - FUCUS VESICULOSUS - GALIUM APARINE WHOLE - HAMAMELIS VIRGINIANA ROOT BARK - LYCOPODIUM CLAVATUM SPORE - MYOSOTIS ARVENSIS - PODOPHYLLUM PELTATUM ROOT - RANCID BEEF - SODIUM SULFATE - SOLIDAGO VIRGAUREA FLOWERING TOP - STRYCHNOS NUX VOMICA SEED - THUJA OCCIDENTALIS LEAFY TWIG -
Manufacturer Guna spa
Product type HUMAN OTC DRUG
SPL set ID af5e3933-4b2f-0966-e053-2995a90aaf2c
SPL ID af5e38c0-3d5d-4733-e053-2a95a90afefe
Version 1
Effective date 2020-09-24
Source export date 2026-10-27
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:39:12 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 · 24 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 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 accidental overdose, seek prfessional assistance or contact a Poison Control Center immediately Contains ethyl alcohol 30%
Adverse reactions cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions sections page 1 of 1 · 1 matching rows.
adverse reactions To Report SUSPECTED ADVERSE REACTIONS, contact Guna Inc at (484) 223-3500 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.