GUNA-HYPERTENSION

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-HYPERTENSION
Generic name: ARNICA MONTANA - FUMARIC ACID - GOLD - LEAD - MELATONIN - MELILOTUS - OLEA EUROPAEA FLOWER - PORK KIDNEY - RAUWOLFIA SERPENTINA - SODIUM PYRUVATE - SPIGELIA - SUS SCROFA ADRENAL GLAND - SUS SCROFA DIENCEPHALON - UBIDECARENONE - VISCUM ALBUM FRUIT -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 40c5b156-dc5c-41c2-88c3-a9bf28119d22
SPL ID: 7e02b61a-2014-7b6d-e053-2991aa0abb80
Version: 2
Effective date: 2018-12-21
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:50

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA-HYPERTENSION	openfda.brand_name
generic name		ARNICA MONTANA - FUMARIC ACID - GOLD - LEAD - MELATONIN - MELILOTUS - OLEA EUROPAEA FLOWER - PORK KIDNEY - RAUWOLFIA SERPENTINA - SODIUM PYRUVATE - SPIGELIA - SUS SCROFA ADRENAL GLAND - SUS SCROFA DIENCEPHALON - UBIDECARENONE - VISCUM ALBUM FRUIT -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-347-18	openfda.package_ndc
ndc	product	17089-347	openfda.product_ndc
ndc11	package	17089034718	derived:openfda.package_ndc
spl id		7e02b61a-2014-7b6d-e053-2991aa0abb80	id
spl set id		40c5b156-dc5c-41c2-88c3-a9bf28119d22	set_id
unii		EJ27X76M46	openfda.unii
unii		88XHZ13131	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		467D26HS0B	openfda.unii
unii		H192N84N1G	openfda.unii
unii		23PJ4252VL	openfda.unii
unii		POD38AIF08	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		X7BCI5P86H	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		2P299V784P	openfda.unii
unii		P83EQ521R3	openfda.unii
unii		498M34P1VZ	openfda.unii
unii		JL5DK93RCL	openfda.unii
unii		F22I9R6Q0X	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. 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.