GUNA BOWEL PLUS

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 PLUS
Generic name: ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE -
Manufacturer: Guna spa
Product type: HUMAN OTC DRUG
SPL set ID: b3aa4fd3-c87a-ccd2-e053-2995a90a46a9
SPL ID: b3aa6401-9af7-b0d5-e053-2995a90a10ef
Version: 1
Effective date: 2021-01-17
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:48

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		GUNA BOWEL PLUS	openfda.brand_name
generic name		ACTIVATED CHARCOAL - ALOE - ALUMINUM OXIDE - BRYONIA ALBA ROOT - CHELIDONIUM MAJUS - COLLINSONIA - FRANGULA ALNUS BARK - LYCOPODIUM CLAVATUM SPORE - POTASSIUM CARBONATE- RHUBARB - STRYCHNOS NUX VOMICA SEED - SILYBUM MARIANUM SEED - SKATOLE - SODIUM CARBONATE - SUS SCROFA PANCREAS - TARAXACUM OFFICINALE - THIAMINE -	openfda.generic_name
manufacturer name		Guna spa	openfda.manufacturer_name
ndc	package	17089-470-18	openfda.package_ndc
ndc	product	17089-470	openfda.product_ndc
ndc11	package	17089047018	derived:openfda.package_ndc
spl id		b3aa6401-9af7-b0d5-e053-2995a90a10ef	id
spl set id		b3aa4fd3-c87a-ccd2-e053-2995a90a46a9	set_id
unii		2P3VWU3H10	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		LMI26O6933	openfda.unii
unii		269XH13919	openfda.unii
unii		S2D77IH61R	openfda.unii
unii		39981FM375	openfda.unii
unii		U946SH95EE	openfda.unii
unii		G280W4MW6E	openfda.unii
unii		9W945B5H7R	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		V5VD430YW9	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		45P3261C7T	openfda.unii
unii		X66NSO3N35	openfda.unii
unii		C88X29Y479	openfda.unii
unii		9Y3J3362RY	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 care professional before use. Keep out of reach of children . In case of accidental overdose, seek professional assitance ot or contact a Poison Control Center immediately Contains Aloe: do not use orally for more than 30 days. Contains ethyl alcohol 30%

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.