GUNA-BOWEL

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-BOWEL
Generic name: ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA COLON - SUS SCROFA RECTUM - TARAXACUM OFFICINALE - THIAMINE -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: 75465821-a889-4697-b470-e9588a523205
SPL ID: 53e95cf4-56b0-8501-e063-6294a90a3edd
Version: 7
Effective date: 2026-06-10
Source export date: 2026-10-27
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/29a1aba6a935d72bab5474118c2ccf25cb52dfe8488fe1593c734ea6c04e3722/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:45:33

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-BOWEL	openfda.brand_name
generic name		ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - CHOLECALCIFEROL - COLLINSONIA - FRANGULA ALNUS BARK - NIACIN - PANTOTHENIC ACID - POTASSIUM CARBONATE - RHUBARB - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - STRYCHNOS NUX-VOMICA SEED - SUS SCROFA COLON - SUS SCROFA RECTUM - TARAXACUM OFFICINALE - THIAMINE -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-293-18	openfda.package_ndc
ndc	product	17089-293	openfda.product_ndc
ndc11	package	17089029318	derived:openfda.package_ndc
spl id		53e95cf4-56b0-8501-e063-6294a90a3edd	id
spl set id		75465821-a889-4697-b470-e9588a523205	set_id
unii		7E889U5RNN	openfda.unii
unii		LMI26O6933	openfda.unii
unii		19F5HK2737	openfda.unii
unii		269XH13919	openfda.unii
unii		2679MF687A	openfda.unii
unii		S2D77IH61R	openfda.unii
unii		94J255A0UC	openfda.unii
unii		39981FM375	openfda.unii
unii		U946SH95EE	openfda.unii
unii		G280W4MW6E	openfda.unii
unii		9W945B5H7R	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		QV1358E70N	openfda.unii
unii		V5VD430YW9	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		45P3261C7T	openfda.unii
unii		1C6V77QF41	openfda.unii
unii		X66NSO3N35	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.