GUNA SINUS PLUS

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 SINUS PLUS
Generic name: ALTHAEA OFFICINALIS LEAF - CALCIUM SULFIDE - COPPER - DRIMIA MARITIMA BULB - ECHINACEA ANGUSTIFOLIA - HYDRASTIS CANADENSIS WHOLE - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR WHOLE - POTASSIUM DICHROMATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: b48c5634-24cf-343e-e053-2995a90a3a9a
SPL ID: b48c5634-24d0-343e-e053-2995a90a3a9a
Version: 1
Effective date: 2021-02-17
Source export date: 2026-10-30
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/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 19:29:24

Harmonized routes table
Harmonized routes
NASAL

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA SINUS PLUS	openfda.brand_name
generic name		ALTHAEA OFFICINALIS LEAF - CALCIUM SULFIDE - COPPER - DRIMIA MARITIMA BULB - ECHINACEA ANGUSTIFOLIA - HYDRASTIS CANADENSIS WHOLE - LOBARIA PULMONARIA - MANGANESE - MERCURIC SULFIDE - ONION - PLANTAGO MAJOR WHOLE - POTASSIUM DICHROMATE - PULSATILLA VULGARIS - SILICON DIOXIDE - SILVER NITRATE - SINUSITISINUM - SUS SCROFA NASAL MUCOSA -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-472-23	openfda.package_ndc
ndc	product	17089-472	openfda.product_ndc
ndc11	package	17089047223	derived:openfda.package_ndc
spl id		b48c5634-24d0-343e-e053-2995a90a3a9a	id
spl set id		b48c5634-24cf-343e-e053-2995a90a3a9a	set_id
unii		789U1901C5	openfda.unii
unii		R763EBH88T	openfda.unii
unii		E2QQV92338	openfda.unii
unii		42Z2K6ZL8P	openfda.unii
unii		3629601H5D	openfda.unii
unii		ID3Z1X61WY	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		95IT3W8JZE	openfda.unii
unii		PQ6CK8PD0R	openfda.unii
unii		W2469WNO6U	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		B575563DM5	openfda.unii
unii		492225Q21H	openfda.unii
unii		T4423S18FM	openfda.unii
unii		ZI0T668SF1	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		D1YM0P5Z2T	openfda.unii
unii		1MBW07J51Q	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, seek professional assistance or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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