GUNA ALLERGY

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 ALLERGY
Generic name: ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: ae6bd80d-2c70-1a3f-e053-2a95a90a2652
SPL ID: b2580118-8598-5057-e053-2a95a90aab4e
Version: 2
Effective date: 2020-10-23
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:35

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.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA ALLERGY	openfda.brand_name
generic name		ADRENALINUM - ALLIUM CEPA - AMMONIUM CARBONICUM - APIS MELLIFICA - ARGENTUM NITRICUM - ARSENICUM ALBUM - CUPRUM ACETICUM - GALPHIMIA GLAUCA - GLANDULA SUPRARENALIS SUIS - HISTAMINUM HYDROCHLORICUM - LUFFA OPERCULATA - MATRICARIA CHAMOMILLA - MUCOSA NASALIS SUIS - NATRUM MURIATICUM - SABADILLA - SCILLA MARITIMA -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-461-18	openfda.package_ndc
ndc	product	17089-461	openfda.product_ndc
ndc11	package	17089046118	derived:openfda.package_ndc
spl id		b2580118-8598-5057-e053-2a95a90aab4e	id
spl set id		ae6bd80d-2c70-1a3f-e053-2a95a90a2652	set_id
unii		3POA0Q644U	openfda.unii
unii		93PH5Q8M7E	openfda.unii
unii		NJ5VT0FKLJ	openfda.unii
unii		3629601H5D	openfda.unii
unii		ID3Z1X61WY	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		C4MO6809HU	openfda.unii
unii		39M11XPH03	openfda.unii
unii		6NAF1689IO	openfda.unii
unii		492225Q21H	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		G0R4UBI2ZZ	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 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 ethyl alcohol 30%

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.