Intestia

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: Intestia
Generic name: ECHINACEA, IRIS VERSICOLOR, URTICA URENS, ARSENICUM ALBUM, BAPTISIA TINCTORIA, BRYONIA, CINCHONA OFFICINALIS, COLLINSONIA CANADENSIS, DIOSCOREA VILLOSA, I ODIUM, IRIS VERSICOLOR, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NATRUM CARBONICUM, NATRUM MURIATICUM, NUX VOMICA, PHOSPHORUS, PODOPHYLLUM PELTATUM, PULSATILLA, RHUS TOXICODENDRON, PYROGENIUM
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9a132c99-7278-f667-e053-2a95a90a3d2b
SPL ID: b5a89c6f-d9d8-6b12-e053-2a95a90a4a80
Version: 2
Effective date: 2020-12-04
Source export date: 2026-10-30
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:59:52

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Intestia	openfda.brand_name
generic name		ECHINACEA, IRIS VERSICOLOR, URTICA URENS, ARSENICUM ALBUM, BAPTISIA TINCTORIA, BRYONIA, CINCHONA OFFICINALIS, COLLINSONIA CANADENSIS, DIOSCOREA VILLOSA, I ODIUM, IRIS VERSICOLOR, LACHESIS MUTUS, LYCOPODIUM CLAVATUM, NATRUM CARBONICUM, NATRUM MURIATICUM, NUX VOMICA, PHOSPHORUS, PODOPHYLLUM PELTATUM, PULSATILLA, RHUS TOXICODENDRON, PYROGENIUM	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4822-1	openfda.package_ndc
ndc	product	55714-4822	openfda.product_ndc
ndc11	package	55714482201	derived:openfda.package_ndc
spl id		b5a89c6f-d9d8-6b12-e053-2a95a90a4a80	id
spl set id		9a132c99-7278-f667-e053-2a95a90a3d2b	set_id
unii		27YLU75U4W	openfda.unii
unii		IWY3IWX2G8	openfda.unii
unii		269XH13919	openfda.unii
unii		2S713A4VP3	openfda.unii
unii		O2630F3XDR	openfda.unii
unii		29SUH5R3HU	openfda.unii
unii		9679TC07X4	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		S003A158SB	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		45P3261C7T	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		I76KB35JEV	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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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