GUNA-MOOD

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-MOOD
Generic name: 5-HYDROXY TRYPTOPHAN,DL - ALFALFA - AVENA SATIVA FLOWERING TOP - LACHESIS MUTA VENOM - PHOSPHORIC ACID - SALIX ALBA BARK - SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI - SEPIA OFFICINALIS JUICE - SEROTONIN - STRYCHNOS IGNATII SEED - SUS SCROFA PINEAL GLAND - SUS SCROFA THYMUS - TRYPTOPHAN -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 3dc2b414-00b6-446c-a81e-3b023322a278
SPL ID: 53e95b31-d0c4-682e-e063-6394a90a8f55
Version: 6
Effective date: 2026-06-10
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:00:06

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 · 21 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA-MOOD	openfda.brand_name
generic name		5-HYDROXY TRYPTOPHAN,DL - ALFALFA - AVENA SATIVA FLOWERING TOP - LACHESIS MUTA VENOM - PHOSPHORIC ACID - SALIX ALBA BARK - SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI - SEPIA OFFICINALIS JUICE - SEROTONIN - STRYCHNOS IGNATII SEED - SUS SCROFA PINEAL GLAND - SUS SCROFA THYMUS - TRYPTOPHAN -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-265-18	openfda.package_ndc
ndc	product	17089-265	openfda.product_ndc
ndc11	package	17089026518	derived:openfda.package_ndc
spl id		53e95b31-d0c4-682e-e063-6394a90a8f55	id
spl set id		3dc2b414-00b6-446c-a81e-3b023322a278	set_id
unii		8DUH1N11BX	openfda.unii
unii		DJO934BRBD	openfda.unii
unii		050QZ2EDK7	openfda.unii
unii		9181P3OI6N	openfda.unii
unii		QDL83WN8C2	openfda.unii
unii		7B69B0BD62	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		760T5R8B3O	openfda.unii
unii		333DO1RDJY	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		MA9CQJ3F7F	openfda.unii
unii		E4GA8884NN	openfda.unii
unii		205MXS71H7	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.