Ruta Graveolens

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: Ruta Graveolens
Generic name: RUTA GRAVEOLENS
Manufacturer: SEVENE USA
Product type: HUMAN OTC DRUG
SPL set ID: a92b2c14-05a3-4d11-908e-c32325b06eb4
SPL ID: 10316818-6a96-faa1-e063-6294a90aa804
Version: 21
Effective date: 2024-01-30
Source export date: 2026-10-12
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:26:42

Harmonized routes table
Harmonized routes
SUBLINGUAL

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 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Ruta Graveolens	openfda.brand_name
generic name		RUTA GRAVEOLENS	openfda.generic_name
manufacturer name		SEVENE USA	openfda.manufacturer_name
ndc	package	76472-1160-1	openfda.package_ndc
ndc	product	76472-1160	openfda.product_ndc
ndc11	package	76472116001	derived:openfda.package_ndc
spl id		10316818-6a96-faa1-e063-6294a90aa804	id
spl set id		a92b2c14-05a3-4d11-908e-c32325b06eb4	set_id
unii		N94C2U587S	openfda.unii

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

WARNINGS: Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

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