GUNA-FEM

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-FEM
Generic name: ADENOSINUM CICLOPHOSPHORICUM - LILIUM TIGRINUM - MELATONIN - SUS SCROFA ADRENAL GLAND - SUS SCROFA CORPUS LUTEUM - SUS SCROFA HYPOTHALAMUS - SUS SCROFA OVARY - SUS SCROFA PANCREAS - SUS SCROFA PINEAL GLAND - SUS SCROFA PITUITARY GLAND - SUS SCROFA THYMUS - THYROID -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 2a41728f-3270-42d7-aa4e-4c4572870d77
SPL ID: 53f5d23c-08d5-fd02-e063-6294a90a3caf
Version: 8
Effective date: 2026-06-11
Source export date: 2026-10-30
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:59:57

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-FEM	openfda.brand_name
generic name		ADENOSINUM CICLOPHOSPHORICUM - LILIUM TIGRINUM - MELATONIN - SUS SCROFA ADRENAL GLAND - SUS SCROFA CORPUS LUTEUM - SUS SCROFA HYPOTHALAMUS - SUS SCROFA OVARY - SUS SCROFA PANCREAS - SUS SCROFA PINEAL GLAND - SUS SCROFA PITUITARY GLAND - SUS SCROFA THYMUS - THYROID -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-231-18	openfda.package_ndc
ndc	product	17089-231	openfda.product_ndc
ndc11	package	17089023118	derived:openfda.package_ndc
spl id		53f5d23c-08d5-fd02-e063-6294a90a3caf	id
spl set id		2a41728f-3270-42d7-aa4e-4c4572870d77	set_id
unii		6RV024OAUQ	openfda.unii
unii		94X749MHSP	openfda.unii
unii		050QZ2EDK7	openfda.unii
unii		47Z05W73EZ	openfda.unii
unii		7B69B0BD62	openfda.unii
unii		L0PFEMQ1DT	openfda.unii
unii		S7YTV04R8O	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		E0399OZS9N	openfda.unii
unii		JL5DK93RCL	openfda.unii
unii		9Y3J3362RY	openfda.unii
unii		N6R0856Z79	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 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.