GUNA LIVER 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 LIVER PLUS
Generic name: SODIUM PYRUVATE - SILYBUM MARIANUM SEED - CHELIDONIUM MAJUS - FUMARIC ACID - PORK LIVER - TARAXACUM OFFICINALE - LYCOPODIUM CLAVATUM SPORE - SODIUM SULFATE - PHOSPHORUS - BERBERIS VULGARIS ROOT BARK
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: ba44c46e-4509-2e4d-e053-2a95a90a9c95
SPL ID: d32e3bbc-f536-6d6f-e053-2995a90aa9f4
Version: 2
Effective date: 2021-12-15
Source export date: 2026-09-28
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/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:07:10

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA LIVER PLUS	openfda.brand_name
generic name		SODIUM PYRUVATE - SILYBUM MARIANUM SEED - CHELIDONIUM MAJUS - FUMARIC ACID - PORK LIVER - TARAXACUM OFFICINALE - LYCOPODIUM CLAVATUM SPORE - SODIUM SULFATE - PHOSPHORUS - BERBERIS VULGARIS ROOT BARK	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-478-20	openfda.package_ndc
ndc	package	17089-478-21	openfda.package_ndc
ndc	product	17089-478	openfda.product_ndc
ndc11	package	17089047820	derived:openfda.package_ndc
ndc11	package	17089047821	derived:openfda.package_ndc
spl id		d32e3bbc-f536-6d6f-e053-2995a90aa9f4	id
spl set id		ba44c46e-4509-2e4d-e053-2a95a90a9c95	set_id
unii		27YLU75U4W	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		88XHZ13131	openfda.unii
unii		0YPR65R21J	openfda.unii
unii		1TH8Q20J0U	openfda.unii
unii		39981FM375	openfda.unii
unii		U946SH95EE	openfda.unii
unii		POD38AIF08	openfda.unii
unii		6EC706HI7F	openfda.unii
unii		C88X29Y479	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

Stop use and ask doctor if symptoms persist more than 5 days or worsen. If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children. Gallstones, occlusion of the bile ducts, jaundice and any other unclear or persistent discomfort in the upper abdomen may be serious. Consult a doctor promptly if any of these symptoms occur If you suffer from liver diseases, you should consult a doctor

Reported adverse events (FAERS/openFDA)#

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