GUNA FEMALE SUPPORT

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 FEMALE SUPPORT
Generic name: LILIUM LANCIFOLIUM WHOLE FLOWERING - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND - SEPIA OFFICINALIS JUICE - ADENOSINE CYCLIC PHOSPHATE - PULSATILLA VULGARIS - SUS SCROFA HYPOTHALAMUS - SUS SCROFA ADRENAL GLAND - SUS SCROFA PANCREAS - MAGNESIUM PHOSPHATE DIBASIC TRIHYDRATE
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: bb22182f-a503-433f-e053-2995a90a2f47
SPL ID: bb2217fc-c752-20b1-e053-2995a90a2562
Version: 1
Effective date: 2021-02-12
Source export date: 2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:47:53

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA FEMALE SUPPORT	openfda.brand_name
generic name		LILIUM LANCIFOLIUM WHOLE FLOWERING - SUS SCROFA OVARY - SUS SCROFA PITUITARY GLAND - SEPIA OFFICINALIS JUICE - ADENOSINE CYCLIC PHOSPHATE - PULSATILLA VULGARIS - SUS SCROFA HYPOTHALAMUS - SUS SCROFA ADRENAL GLAND - SUS SCROFA PANCREAS - MAGNESIUM PHOSPHATE DIBASIC TRIHYDRATE	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-501-18	openfda.package_ndc
ndc	product	17089-501	openfda.product_ndc
ndc11	package	17089050118	derived:openfda.package_ndc
spl id		bb2217fc-c752-20b1-e053-2995a90a2562	id
spl set id		bb22182f-a503-433f-e053-2995a90a2f47	set_id
unii		QDL83WN8C2	openfda.unii
unii		HF539G9L3Q	openfda.unii
unii		L0PFEMQ1DT	openfda.unii
unii		S7YTV04R8O	openfda.unii
unii		X67Z2963PI	openfda.unii
unii		398IYQ16YV	openfda.unii
unii		E0399OZS9N	openfda.unii
unii		I76KB35JEV	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 worsen or persist more than 5 days. If pregnant or breast-feeding ask a health care professional before use. Keep out of reach of children. In case of accidental overdose, seek 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.