GUNA-DIZZY

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-DIZZY
Generic name: .ALPHA.-KETOGLUTARIC ACID - AMBERGRIS - ANAMIRTA COCCULUS SEED - CONIUM MACULATUM FLOWERING TOP - EPINEPHRINE - FUMARIC ACID - MALIC ACID - MELATONIN - MINERAL OIL - PTERIDIUM AQUILINUM ROOT - PYRIDOXINE HYDROCHLORIDE - QUINHYDRONE - QUININE - SUS SCROFA ARTERY - SUS SCROFA CEREBELLUM - SUS SCROFA PLACENTA - THIAMINE HYDROCHLORIDE - TOBACCO LEAF -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: c5f4a798-e628-4388-a98d-7449dd92f2d6
SPL ID: 7e7be278-8d19-71c4-e053-2991aa0a377c
Version: 3
Effective date: 2018-12-21
Source export date: 2026-10-27
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/eeb012fd0992efa4f76b2aef09dd5f84150b96392c46717c44deabcc4e3581c1/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:39:20

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 · 26 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA-DIZZY	openfda.brand_name
generic name		.ALPHA.-KETOGLUTARIC ACID - AMBERGRIS - ANAMIRTA COCCULUS SEED - CONIUM MACULATUM FLOWERING TOP - EPINEPHRINE - FUMARIC ACID - MALIC ACID - MELATONIN - MINERAL OIL - PTERIDIUM AQUILINUM ROOT - PYRIDOXINE HYDROCHLORIDE - QUINHYDRONE - QUININE - SUS SCROFA ARTERY - SUS SCROFA CEREBELLUM - SUS SCROFA PLACENTA - THIAMINE HYDROCHLORIDE - TOBACCO LEAF -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-306-18	openfda.package_ndc
ndc	product	17089-306	openfda.product_ndc
ndc11	package	17089030618	derived:openfda.package_ndc
spl id		7e7be278-8d19-71c4-e053-2991aa0a377c	id
spl set id		c5f4a798-e628-4388-a98d-7449dd92f2d6	set_id
unii		8ID597Z82X	openfda.unii
unii		6DY04L71DR	openfda.unii
unii		P4A66LQ3QJ	openfda.unii
unii		88XHZ13131	openfda.unii
unii		C8CV8867O8	openfda.unii
unii		Q28R5GF371	openfda.unii
unii		T5L8T28FGP	openfda.unii
unii		6YR2608RSU	openfda.unii
unii		HQJ5Z3SOIV	openfda.unii
unii		YKH834O4BH	openfda.unii
unii		817L1N4CKP	openfda.unii
unii		63O327782Q	openfda.unii
unii		XTC0D02P6C	openfda.unii
unii		M572600E5P	openfda.unii
unii		810258W28U	openfda.unii
unii		68Y4CF58BV	openfda.unii
unii		JL5DK93RCL	openfda.unii
unii		49NGK53TPQ	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.