GUNA KIDNEY 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 KIDNEY PLUS
Generic name: CALCIUM SULFIDE - CHONDRODENDRON TOMENTOSUM ROOT - EQUISETUM HYEMALE - SUS SCROFA PITUITARY GLAND - APIS MELLIFERA - URTICA URENS - SODIUM CHLORIDE - LOBARIA PULMONARIA - HORSE CHESTNUT - BERBERIS VULGARIS FRUIT - SOLIDAGO VIRAGAUREA FLOWERING TOP -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: b8dacd94-8da1-4a8d-e053-2995a90acb67
SPL ID: ba7eb1a4-9059-c47c-e053-2a95a90a6cce
Version: 2
Effective date: 2021-02-04
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:35

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA KIDNEY PLUS	openfda.brand_name
generic name		CALCIUM SULFIDE - CHONDRODENDRON TOMENTOSUM ROOT - EQUISETUM HYEMALE - SUS SCROFA PITUITARY GLAND - APIS MELLIFERA - URTICA URENS - SODIUM CHLORIDE - LOBARIA PULMONARIA - HORSE CHESTNUT - BERBERIS VULGARIS FRUIT - SOLIDAGO VIRAGAUREA FLOWERING TOP -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-474-18	openfda.package_ndc
ndc	product	17089-474	openfda.product_ndc
ndc11	package	17089047418	derived:openfda.package_ndc
spl id		ba7eb1a4-9059-c47c-e053-2a95a90a6cce	id
spl set id		b8dacd94-8da1-4a8d-e053-2995a90acb67	set_id
unii		395A3P448Z	openfda.unii
unii		6XEF22AHC3	openfda.unii
unii		3C18L6RJAZ	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		L0PFEMQ1DT	openfda.unii
unii		59677RXH25	openfda.unii
unii		7S82P3R43Z	openfda.unii
unii		5405K23S50	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, get 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.