GUNA-REFLUX

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-REFLUX
Generic name: ACTIVATED CHARCOAL - AETHUSA CYNAPIUM - APOMORPHINE HYDROCHLORIDE - BRYONIA ALBA ROOT - COLCHICUM AUTUMNALE BULB - IPECAC - LYCOPODIUM CLAVATUM SPORE - STRYCHNOS IGNATII SEED - STRYCHNOS NUX-VOMICA SEED - WATERMELON - SUS SCROFA STOMACH -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 444c1f4c-dd0c-4525-bb65-c0c211c9487f
SPL ID: 7e8f7213-7f81-14ab-e053-2991aa0a4669
Version: 3
Effective date: 2018-12-21
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:48

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-REFLUX	openfda.brand_name
generic name		ACTIVATED CHARCOAL - AETHUSA CYNAPIUM - APOMORPHINE HYDROCHLORIDE - BRYONIA ALBA ROOT - COLCHICUM AUTUMNALE BULB - IPECAC - LYCOPODIUM CLAVATUM SPORE - STRYCHNOS IGNATII SEED - STRYCHNOS NUX-VOMICA SEED - WATERMELON - SUS SCROFA STOMACH -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-406-18	openfda.package_ndc
ndc	product	17089-406	openfda.product_ndc
ndc11	package	17089040618	derived:openfda.package_ndc
spl id		7e8f7213-7f81-14ab-e053-2991aa0a4669	id
spl set id		444c1f4c-dd0c-4525-bb65-c0c211c9487f	set_id
unii		2P3VWU3H10	openfda.unii
unii		T0920P9Z9A	openfda.unii
unii		269XH13919	openfda.unii
unii		993QHL78E6	openfda.unii
unii		81FZ7X4MWD	openfda.unii
unii		1NM3M2487K	openfda.unii
unii		F39049Y068	openfda.unii
unii		M6936L953C	openfda.unii
unii		62I3C8233L	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		231473QB6R	openfda.unii
unii		C88X29Y479	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.