GUNA-DERMO

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-DERMO
Generic name: ALDESLEUKIN - ARSENIC TRIOXIDE - ATROPA BELLADONNA - CANAKINUMAB - ECHINACEA ANGUSTIFOLIA - GRAPHITE - MELATONIN - PLANTAGO MAJOR - SOLANUM DULCAMARA FLOWER - SULFUR -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 8bf717eb-fe46-4066-b124-eb715ffc1542
SPL ID: 7e8f7213-7f6e-14ab-e053-2991aa0a4669
Version: 2
Effective date: 2018-12-21
Source export date: 2026-10-30
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/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:22:42

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.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA-DERMO	openfda.brand_name
generic name		ALDESLEUKIN - ARSENIC TRIOXIDE - ATROPA BELLADONNA - CANAKINUMAB - ECHINACEA ANGUSTIFOLIA - GRAPHITE - MELATONIN - PLANTAGO MAJOR - SOLANUM DULCAMARA FLOWER - SULFUR -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-295-18	openfda.package_ndc
ndc	product	17089-295	openfda.product_ndc
ndc11	package	17089029518	derived:openfda.package_ndc
spl id		7e8f7213-7f6e-14ab-e053-2991aa0a4669	id
spl set id		8bf717eb-fe46-4066-b124-eb715ffc1542	set_id
unii		4QQN74LH4O	openfda.unii
unii		37CQ2C7X93	openfda.unii
unii		W2469WNO6U	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		M89N0Q7EQR	openfda.unii
unii		W6J1279A6K	openfda.unii
unii		WQZ3G9PF0H	openfda.unii
unii		70FD1KFU70	openfda.unii
unii		JL5DK93RCL	openfda.unii

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 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.